Idaho Firm Recalls Kratom Product After State Lab Finds Salmonella

Vanguard Enterprises, LLC. DBA Bedrock MFG of Boise, Idaho is recalling Monarch Premium Kratom brand Bali Gold, Red Bali, Green Maeng Da, and White Elephant powder because product has the potential to be contaminated with Salmonella.  This recall is the result of a retail sample collected and analyzed by the Florida Department of Agriculture & Consumer Services (FDACS) which revealed that the finished product contained Salmonella

The affected Monarch Premium Kratom brand Bali Gold, Red Bali, Green Maeng Da, and White Elephant powder were distributed nationwide in retail stores and through mail orders via the company website https://bedrockbotanicals.com between April 2023 to September 2023.

From the DEA https://www.dea.gov/sites/default/files/2020-06/Kratom-2020_0.pdf

What is Kratom - Kratom is a tropical tree native to Southeast Asia. Consumption of its leaves produces both stimulant effects (in low doses) and sedative effects (in high doses), and can lead to psychotic symptoms, and psychological and physiological dependence. Kratom leaves  contain two major psychoactive ingredients (mitragynine and  7-hydroxymytragynine). These leaves are crushed and then smoked, brewed with tea, or placed into gel capsules. Kratom has a long history of use in Southeast Asia

Mostly abused by oral ingestion in the form of a tablet, capsule, or extract. Kratom leaves may also be dried or powdered and ingested as a tea, or the kratom leaf may be chewed.

Kratom is not controlled under the Controlled Substances Act; however, there may be some state regulations or prohibitions against the possession and use of kratom. The FDA has not approved kratom 

for any medical use. In addition, DEA has listed kratom as a Drug and Chemical of Concern.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vanguard-enterprises-llc-dba-bedrock-mfg-recalls-monarch-premium-kratom-powder-because-possible
Vanguard Enterprises, LLC. dba Bedrock MFG Recalls Monarch Premium Kratom Powder Because of Possible Health Risk
Summary
Company Announcement Date:  October 30, 2025
FDA Publish Date:  October 31, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential to be contaminated with Salmonella
Company Name:  Vanguard Enterprises, LLC. DBA Bedrock MFG
Brand Name:  Monarch Premium
Product Description:  Bali Gold, Red Bali, Green Maeng Da, and White Elephant Kratom powder

CA Fruit Packer is Recalling Fresh Peaches After Listeria Found in Packing Facility

Moonlight Companies, Reedley, CA  is voluntarily recalling California-grown conventional yellow and white peaches because they have the potential to be contaminated with Listeria monocytogenes.  This recall is being conducted because Listeria monocytogenes was identified in the packing facility environment.

The recalled peaches were sold at retail stores nationwide between September 16, 2025 and October 29, 2025. 

This is a very big production window of time leading one to believe it was the time interval of sampling in the facility.  This is where a well thought out sampling strategy is so important. 

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/moonlight-companies-voluntarily-recalls-california-grown-conventional-yellow-and-white-peaches
Moonlight Companies Voluntarily Recalls California-Grown Conventional Yellow and White Peaches Because of Possible Health Risk
Summary
Company Announcement Date:  October 29, 2025
FDA Publish Date:  October 30, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential to be contaminated with Listeria monocytogenes.
Company Name:  Moonlight Companies
Brand Name:  Moonlight/Kroger
Product Description:  Yellow and white peaches

FDA and CDC Provide Update (Oct 30 2025) on Listeria Outbreak Linked to Pre-cooked Pasta

FDA issued an update on the Listeria outbreak linked to pre-cooked pasta produced by Nate's Fine Foods of Roseville, CA and which was used as an ingredient by a number of other companies in making RTE dishes.  As of 10/30/25, there have been 27 reported cases with 25 hospitalizations and 6 deaths.
From the CDC report of 10/30/25, the age range of those infected is from 4 to 92 years, with a median age of 74.  From the CDC, "Of 26 people with information available, 25 have been hospitalized and 6 deaths have been reported. One death from each of the following states: Hawaii, Illinois, Michigan, Oregon, Texas, and Utah. One pregnancy-associated illness resulted in a fetal loss."

Case Counts
Total Illnesses: 27
Hospitalizations: 25
Deaths: 6
Last Illness Onset: October 16, 2025
States with Cases: CA, FL, HI, IL, IN, LA, MI, MN, MO, NC, NV, OH, OR, SC, TX, UT, VA, WA
Product Distribution: Nationwide

The outbreak was first reported in June with the last report coming in September, 2025 with 7 new cases and 2 additional deaths.  

An investigative report has not been issued yet, but we did overview where some of controls were needed.

FDA
https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-listeria-monocytogenes-prepared-pasta-meals-june-2025
Outbreak Investigation of Listeria monocytogenes: Prepared Pasta Meals (June 2025)
Do not eat or serve certain pasta salads or meals containing pre-cooked pasta. FDA’s investigation is ongoing.
Current Update
October 30, 2025

FDA Issues Warning Letters for Improper Implementation of FSVP

FDA issued Warning Letters to two importers for failure to properly implement FSVP.  The Turkana Foods case below is a great example of failure to complete corrective action once a foodborne illness outbreak occurs from a given supplier.

V & L Produce, Inc. ,Vernon, CA did not develop an FSVP for any of the foods imported, including each of the following foods:

• Jalapeno Pepper, imported from (b)(4), located in (b)(4)
• Green Onions, imported from (b)(4), located in (b)(4)
• Husk Tomatoes (Tomatillos), imported from (b)(4), located in (b)(4)

The imported fresh produce that may be considered “covered produce” as defined in 21 CFR 112.3. If after review of the fresh produce that is imported, one determines that they importer covered produce, one must have an FSVP that demonstrates that the supplier is producing the food in compliance with processes and procedures that provide at least the same level of public health protection as those required under section 419 of the FD&C Act (21 U.S.C. 350h) (regarding standards for produce safety) and the implementing regulations in the Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption (21 CFR part 112).

Turkana Food Inc., Kenilworth, NJ, was not in compliance with the requirements of 21 CFR part 1, subpart L for the following imported foods: Tahini, Halva with Vanilla, Halva with Cocoa and Halva with Pistachio from (b)(4), Tahini from (b)(4), and Crushed Hot Red Pepper Spice
Corrective Actions in Response to a Salmonella Outbreak -  The firm failed to properly respond to product that was involved in a salmonella outbreak.  

• The firm recalled Tahini manufactured by (b)(4) in (b)(4) that was found to contain Salmonella in February 2025, but  did not provide any documentation to show that it took corrective actions as a result of the Salmonella finding. Under 21 CFR 1.508(a), the appropriate corrective actions will depend on the circumstances but could include discontinuing use of the foreign supplier until the cause or causes of noncompliance, adulteration, or misbranding have been adequately addressed.
• Did not provide any documentation of your investigation to determine if the FSVP is adequate after Tahini manufactured by (b)(4) in (b)(4) was recalled in February 2025.
• After Tahini from (b)(4) was recalled in February 2025, the company continued to import product including Halva with Pistachio, Halva with Vanilla, and Halva with Cocoa which all contain Tahini on April 8, 2025, from the same foreign supplier. 
• There were additional elements of corrective action that were also not taken.

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/v-l-produce-inc-717804-10092025
V & L Produce, Inc.
MARCS-CMS 717804 — October 09, 2025

NY Firm Recalls Dried Uneviscerated Fish

New Hoque & Sons Inc. of Maspeth, NY, is recalling its packages of “Dry Ghoinnya Fish” because the product was found to be uneviscerated.  The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory staff revealed the product was not properly eviscerated prior to processing.  The sale of uneviscerated fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish have been linked to outbreaks of botulism poisoning.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/new-hoque-sons-inc-issues-alert-uneviscerated-dry-ghoinnya-fish
New Hoque & Sons Inc Issues Alert on Uneviscerated “Dry Ghoinnya Fish”
Summary
Company Announcement Date:  October 29, 2025
FDA Publish Date:  October 29, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Product was found to be uneviscerated. Uneviscerated fish have been linked to outbreaks of botulism poisoning.
Company Name:  New Hoque & Sons Inc.
Brand Name:  Hoque
Product Description:  Dry Ghoinnya Fish

Company Announcement

New Hoque & Sons Inc. of Maspeth, NY, is recalling its packages of “Dry Ghoinnya Fish” because the product was found to be uneviscerated.

The recalled “Dry Ghoinnya Fish” were distributed nationwide in retail stores. The product comes in a 10-12 pound, clear plastic package marked with an expiration date of 5/19/25 stamped on the bottom. The product UPC code is 908172635412.

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory staff revealed the product was not properly eviscerated prior to processing.

The sale of uneviscerated fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish have been linked to outbreaks of botulism poisoning. Symptoms of botulism include dizziness, blurred or double vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension, and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.

No illnesses have been reported to date in connection with this problem.

Consumers who have purchased the “Dry Ghoinnya Fish” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (718) 391-0992.

Massachusetts Firm Misses Allergen on Print-on-Demand Label

Hampton Farms, Springfield, Mass.,  is recalling Mixed Nuts Roasted Unsalted 8 oz. lot 23025  and Mixed Nuts Roasted and Salted 8oz. lot 23825 due to an undeclared hazelnut allergen.  On September 15, 2025, the firm discovered through routine paperwork review that the label failed to include the allergen (hazelnuts) in the allergen warning statement.

Here is another case related to print-on-demand labels where there is an allergen mistake.  The information input on these labels needs a sufficient amount of review / verification instead of relying on one person.

The products were distributed between September 2, 2025 and September 9, 2025 of this year. These products were packaged in clear plastic tubs and sold in Stop&Shop stores in Massachusetts, Connecticut, New Jersey, New York and Rhode Island


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hampton-farms-recalls-mixed-nuts-roasted-unsalted-8-oz-and-mixed-nuts-roasted-and-salted-8-oz
Hampton Farms Recalls Mixed Nuts Roasted Unsalted 8 oz and Mixed Nuts Roasted and Salted 8 oz Packages Due to Undeclared Hazelnuts
Summary
Company Announcement Date:   September 26, 2025
FDA Publish Date:  October 28, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared hazelnut allergen
Company Name:  Hampton Farms
Brand Name:  Hampton Farms
Product Description:  Mixed Nuts

TX Firm Recalls Taco Kits After Supplier Mislabels Cocoa Packets As Seasoning Packet

Teasdale Foods, Inc., Carrollton, TX, is recalling certain Taco Dinner Kits, because they may contain undeclared milk.  The recall was initiated after the company received consumer complaints the Taco Dinner Kits contained cocoa mix packets containing milk instead of taco seasoning packets and were distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicates the problem was caused by mislabeling of the taco seasoning packets by the third party that provides the seasoning.

In this case, the supplier of the taco seasoning packets mislabeled cocoa packets as taco seasoning.  Here is a great example of the need to ensure suppliers have tight allergen control programs in place.  Clearly this supplier is handling a wide variety of foods containing different allergens.

Product was distributed to Giant, Martin’s, and Aldi retail stores located in Alabama, Connecticut, District of Columbia, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Mississippi, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Virginia, Vermont, Wisconsin and West Virginia.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teasdale-latin-foods-issues-allergy-alert-potential-undeclared-milk-certain-taco-dinner-kits
Teasdale Latin Foods Issues Allergy Alert on Potential Undeclared Milk in Certain Taco Dinner Kits
Summary
Company Announcement Date:  October 25, 2025
FDA Publish Date:  October 28, 2025
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared milk.
Company Name:  Teasdale Foods, Inc.
Brand Name:  Martin’s and Giant/Casa Mamita
Product Description:  Taco Dinner Kits

CA Distributor Recalls Parsley After Sample Tests Positive for Salmonella

Pacific International Marketing (“Pacific”), a Salinas, California distributor, is recalling 474 cases of bulk Italian Parsley because it may be contaminated with Salmonella.  The company was recently notified that a sample taken on October 6 tested positive. This product should no longer be available directly to the consumer, only if the product is frozen.

The Italian Parsley was shipped to wholesalers in AZ, CA, FL, MN, MI, GA, OH and NV between September 22 and September 25, 2025. 


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pacific-international-marketing-recalls-fresh-italian-parsley-because-possible-health-risk
Pacific International Marketing Recalls Fresh Italian Parsley Because of Possible Health Risk
Summary
Company Announcement Date:  October 28, 2025
FDA Publish Date:  October 28, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness – Salmonella contamination
Company Name:  Pacific International Marketing
Brand Name:  Pacific
Product Description:  Italian Parsley

WA State Company Recalls Cinnamon Powder After FDA Finds Lead Contamination

Homeneeds Inc. of Bellevue, WA is recalling 140/100gram packets of Devi brand Cinnamon Powder (Dalchini Powder), batch #2502315, because it has the potential to be contaminated with lead.  The recall was initiated after the FDA collected product samples and detected elevated levels of lead. The firm’s investigation into the problem is ongoing.

The affected Devi brand Cinnamon Powder (Dalchini Powder) packages were distributed by Homeneeds Inc. of Bellevue, WA and was sold at Apna Bazar in WA from 05/15/2025 to 10/21/2025


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/homeneeds-inc-recalls-devi-brand-ground-cinnamon-dalchini-powder-because-possible-health-risk
Homeneeds Inc. Recalls Devi Brand Ground Cinnamon (Dalchini Powder) Because of Possible Health Risk
Summary
Company Announcement Date:  October 27, 2025
FDA Publish Date:  October 28, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential Metal Contaminant - Lead
Company Name:  Homeneeds Inc.
Brand Name:  DEVI
Product Description:  Ground Cinnamon

MN Establishment Recalls Pulled Pork Product After Plastic from Ingredient Bottles Found in Product

E.A. Sween Company, an Eden Prairie, Minn. establishment, is recalling approximately 127,887 pounds of a pulled pork sandwich product that may be contaminated with pieces of plastic.  The problem was discovered after the establishment received multiple complaints from consumers finding pieces of plastic in the barbecue pulled pork sandwich product. E.A. Sween Company determined that the plastic originated from the gallon plastic barbecue bottles used in production.

This recall demonstrates the need to control ingredient containers during production.  It is easy for people to get careless when pouring liquid into the process in that they do not control have full containment of items including the caps.


https://www.fsis.usda.gov/recalls-alerts/e-a--sween-company-recalls-pulled-pork-sandwich-products-due-possible-foreign-matter
E.A. Sween Company Recalls Pulled Pork Sandwich Products Due to Possible Foreign Matter Contamination

WASHINGTON, Oct. 27, 2025 – E.A. Sween Company, an Eden Prairie, Minn. establishment, is recalling approximately 127,887 pounds of a pulled pork sandwich product that may be contaminated with pieces of plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

Source of Cesium-137 in Shipments of Indonesian Frozen Shrimp Determined

An article in Food Safety News state the the source of the Cesium-137 that was detected in a shipment of frozen shrimp that led to tightened controls for Indonesian products over the past few months.  According to this article, the "contamination was allegedly caused by steel manufacturer Peter Metal Technology, which uses imported scrap metal as its primary raw material. It is likely that the cesium was incorporated into the firm’s waste stream and then processed, releasing Cs-137 particles into the air, which may have spread to nearby shrimp packaging facility PT Bahari Makmur Sejati (doing business as BMS Foods), located approximately two kilometers away."

"The American Nuclear Society explained that the Cs-137 contamination likely began as cesium chloride, which, once smelted, would rise above its boiling point and enter the atmosphere in gaseous form, exposing BMS Foods' facility to the radioactive isotope."

"Additionally, the Indonesian government discovered 14 containers of scraps from the Philippines, which are contaminated by Cs-137, in Tanjung Priok Port, North Jakarta. This finding suggests that the radioactive contamination may also originate to containers used in export, as well as from the Cikande environment."

This explanation does not apply to the shipment of cloves that were also found to have Cesium-137 contamination.

Food Safety Magazine
https://www.food-safety.com/articles/10757-indonesian-officials-find-cause-of-cs-137-contamination-behind-radioactive-shrimp
Indonesian Officials Find Cause of Cs-137 Contamination Behind Radioactive Shrimp

October 6, 2025

Since August, the U.S. Food and Drug Administration (FDA) has alerted the public to detections of radioactive isotope Cesium-137 (Cs-137) in shipments of shrimp sold at Walmart and other major retailers, and clove spices that did not enter commerce, imported from Indonesia. These detections led FDA to exercise for the first time a Congressional authorized power to require import certification for those commodities from certain regions of the country.

Raw Milk Cheese from Washington State Recalled After Linked to Three Cases of E. coli (STEC) Infection

A Washington cheese maker is recalling various cheese products made from raw and unpasteurized milk and aged at least 60 days, after the product was linked to illness from Shiga toxin-producing Escherichia coli (STEC), specifically Escherichia coli O103.

Twin Sisters Creamery of Ferndale, Washington is voluntarily recalling Whatcom Blue, Farmhouse, Peppercorn and Mustard Seed cheese products, which were made from raw and unpasteurized milk and aged at least 60 days, because it may be contaminated with Shiga toxin-producing Escherichia coli (STEC) and Escherichia coli O103

There have been three reports of STEC infections caused by E. coli O103 in OR and WA to date. The case in Oregon consumed the Twin Sisters Creamery Farmhouse cheese prior to becoming ill.  The recall was initiated after Twin Sisters Creamery was notified that the Farmhouse cheese sample analyzed by a third-party lab confirmed presence of E. coli O103 and E. Coli STEC was detected in Whatcom Blue samples analyzed by WSDA and FDA.

Peterson Company of Auburn, WA is voluntarily recalling Twin Sisters Creamery brand item# 28855 Whatcom Blue and item# 29608 Farmhouse Cheese products which were made by Twin Sisters.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/twin-sisters-creamery-recalls-whatcom-blue-farmhouse-peppercorn-and-mustard-seed-cheese-products

Twin Sisters Creamery Recalls Whatcom Blue, Farmhouse, Peppercorn, and Mustard Seed Cheese Products Because of Possible Health Risk

Summary

Company Announcement Date:  October 25, 2025

FDA Publish Date:  October 27, 2025

Product Type:  Food & Beverages

Reason for Announcement:  Potential Foodborne Illness - Shiga toxin-producing Escherichia coli (STEC) and Escherichia coli O103

Company Name:  Twin Sisters Creamery, Inc.

Brand Name:  Twin Sisters Creamery

Product Description: Whatcom Blue, Farmhouse, Peppercorn and Mustard Seed cheese products

Michigan Firm Recalls Chocolate Bars for Undeclared Nuts Due to Processing Error

Zingerman’s Candy Manufactory of Ann Arbor, Michigan is recalling Zingerman’s Peanut Butter Crush Full Size Bars with Lot#174250 because it may contain undeclared cashew and Zingerman’s Ca$hew Cow Full Size Bars with Lot#174250 because it may contain undeclared peanut.  The recall was initiated after it was discovered that Peanut Butter Crush Bars containing cashews were distributed in packaging that did not reveal the presence of cashews. It was also discovered that Cashew Cow Bars may have been distributed in packaging that did not reveal the presence of peanuts. Subsequent investigation indicates the problem was caused by a temporary breakdown in the production and packaging processes.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/zingermans-candy-manufactory-issues-allergy-alert-undeclared-peanut-cashew-candy-bars
Zingerman’s Candy Manufactory Issues Allergy Alert on Undeclared Peanut & Cashew in Candy Bars
Summary
Company Announcement Date:  October 24, 2025
FDA Publish Date:  October 27, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential or Undeclared Allergen – Undeclared Cashew and Peanut
Company Name:  Zingerman’s Candy Manufactory
Brand Name:  Zingerman’s Candy
Product Description:  Peanut Butter Crush and Ca$hew Cow candy bars

MN Establishment Recalls Frozen RTE Chicken Breast After Complaints for Metal Originating with Conveyor Belts

Hormel Foods Corporation, an Austin, Minn. establishment, is recalling approximately 4,874,815 pounds of foodservice ready-to-eat frozen chicken products that may be contaminated with pieces of metal,  The problem was discovered after the establishment received multiple complaints from foodservice customers finding metal in their frozen chicken breast and chicken thigh products. Hormel Foods determined that the metal originated from the conveyor belt used in production.

The affected chicken breast and thigh products were distributed to HRI Commercial Food Service locations nationwide on various dates from February 10, 2025, through September 19, 2025.  There have been no confirmed reports of injury due to consumption of this product. 


https://www.fsis.usda.gov/recalls-alerts/hormel-foods-corporation-recalls-ready-eat-frozen-chicken-products-due-possible
Hormel Foods Corporation Recalls Ready-To-Eat Frozen Chicken Products Due to Possible Foreign Matter Contamination

FSIS Announcement

WASHINGTON, October 25, 2025 – Hormel Foods Corporation, an Austin, Minn. establishment, is recalling approximately 4,874,815 pounds of foodservice ready-to-eat frozen chicken products that may be contaminated with pieces of metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

SD Establishment Recalls Pork Jerky After Metal from Fraying Belt Found in Product

LSI, Inc., an Alpena, S.D. establishment, is recalling approximately 2,277,540 pounds of a ready-to-eat Korean barbecue pork jerky product that may be contaminated with pieces of metal.  The problem was discovered after the establishment received multiple complaints from consumers finding pieces of wiry metal in the pork jerky product. LSI, Inc. determined that the metal originated from the conveyor belt used in production. 

This item was shipped to Costco and Sam’s Club retail locations nationwide.  There have been no confirmed reports of injury due to consumption of this product. 

https://www.fsis.usda.gov/recalls-alerts/lsi-inc--recalls-bbq-pork-jerky-product-due-possible-foreign-matter-contamination
LSI, Inc. Recalls BBQ Pork Jerky Product Due To Possible Foreign Matter Contamination

LSI, Inc.

FSIS Announcement

WASHINGTON, October 24, 2025 – LSI, Inc., an Alpena, S.D. establishment, is recalling approximately 2,277,540 pounds of a ready-to-eat Korean barbecue pork jerky product that may be contaminated with pieces of metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

Europe - Invesitigation into Salmonella Outbreak Linked to Tomatoes 2011 - 2024

An investigation report in Eurosurveillance details a Salmonella outbreak linked to cherry tomatoes occurring from 2011 to 2024 with 643 reported cases in 17 countries.   First notice that a common food, cherry tomatoes, was identified in 2023, but reported cases continued into 2024 with 132 occurring that year.   Eventually, tomatoes from Sicily were identified as the vehicle, but the exact source was not identified.

"Contamination of tomatoes can happen at various points from the farm-to-fork, such as farm, packinghouses, or fresh-cut processing facilities [26]. They can potentially become contaminated with faeces from wild animals [29] or migratory birds [30,31]. Since water used for irrigation does not need to be potable, this may be a further source of contamination. Additionally, during water restrictions, different types of water can be used. Surface waters, such as rivers, streams or lakes, are more susceptible to contamination than protected sources like wells. The sewage sludge isolates from Germany and Austria support the hypothesis that sewage water can carry harmful pathogens and could be transferred to crops when used for irrigation or applied as a fertiliser [21]."

Eurosurveillance Volume 30, Issue 41, 16/Oct/2025
https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2025.30.41.2500224
Insights into recurring multi-country outbreaks of Salmonella Strathcona associated with tomatoes, Europe, 2011 to 2024

Introduction

In 2023, non-typhoidal salmonellosis was the second most frequently reported gastrointestinal infection among humans in the European Union and European Economic Area (EU/EEA) countries after campylobacteriosis, accounting for 78,307 cases reported by 30 EU/EEA countries with an incidence of 18.15 cases per 100,000 population [1]. Notification of non-typhoidal salmonellosis is mandatory in 27 EU/EEA countries [1], while in three countries (Belgium, France and the Netherlands), it is voluntary [2]. Non-typhoidal salmonellosis is characterised by diarrhoea, abdominal pain and fever. In some cases, infections may become invasive causing bacteraemia and sepsis, requiring hospitalisation and antimicrobial treatment [3]. The most frequently notified Salmonella enterica subspecies enterica (S.) serovars in humans in the EU/EEA countries are Enteritidis and Typhimurium, including monophasic Typhimurium [2,4].

CA Establishment Recalls RTE Burrito Products After RTE Egg Ingredient Tests Positive for Listeria

M.C.I. Foods Inc., a Santa Fe Springs, Calif., establishment, is recalling approximately 91,585 pounds of specific lots of ready-to-eat (RTE) breakfast burrito and wrap products containing egg that may be adulterated with Listeria monocytogenes (Lm).  The problem was discovered when the establishment notified FSIS of a positive Lm result in the scrambled egg component after the firm conducted routine sampling and testing of RTE ingredients from its external suppliers.

USDA does not require a Supply Chain Preventive Control as is required by FDA, however, the same types of controls need to be in place for suppliers of  RTE ingredients.  While testing was in place and did identify the contamination, which is good, however, the goal is prevention rather than reacting.  In this case, the product had been released and now has to be recalled.  In a preventive control's approach, the purchasing company would verify control through audits, prior testing communicated by a COA, or even an evaluation of that supplier's environmental monitoring program.

There have been no confirmed reports of illness due to consumption of these products.


https://www.fsis.usda.gov/recalls-alerts/m-c-i--foods-inc--recalls-ready-eat-breakfast-burrito-and-wrap-products-due-possible
M.C.I. Foods, Inc. Recalls Ready-To-Eat Breakfast Burrito and Wrap Products Due to Possible Listeria Contamination

WASHINGTON, October 18, 2025 – M.C.I. Foods Inc., a Santa Fe Springs, Calif., establishment, is recalling approximately 91,585 pounds of specific lots of ready-to-eat (RTE) breakfast burrito and wrap products containing egg that may be adulterated with Listeria monocytogenes (Lm), the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

CA Firm Recalls Cinnamon Powder After FDA Testing Detects Lead

Haitai, Inc of Cerritos, CA (Oct., 15, 2025) is recalling Haetae (HT) brand Cinnamon powder 8 oz because it has the potential to be contaminated with lead.  The recall was initiated after the FDA collected product samples and detected elevated levels of lead. The firm’s investigation indicates the problem might be caused by potentially adulterated raw material from the supplier or natural lead concentration in Cinnamon and its powder.

Product was distributed by Haitai, Inc. and sold at various supermarkets nationwide.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haitai-inc-recalls-haetae-ht-brand-cinnamon-powder-8-oz-possible-risk
Haitai, Inc. Recalls Haetae (HT) Brand Cinnamon Powder 8 oz of Possible Risk
Summary
Company Announcement 

Date: October 17, 2025

FDA Publish Date: October 17, 2025

Product Type: Food & Beverages

Reason for Announcement:  Potential Metal Contaminant - Lead

Company Name: Haitai, Inc

Brand Name:  Haetae

Product Description:  Ground cinnamon
Company Announcement

NY Firm Recalls Pecan Product for Undeclared Cashews

Nat’s Nuts of Rochester, NY is recalling 600 bags of Cinnamon Whiskey Pecans, because they may contain undeclared cashews. People who have an allergy or severe sensitivity to cashews run the risk of serious or life-threatening allergic reaction if they consume these products.  The recall was initiated after a retailer opened a package of the Cinnamon Whiskey Pecans for sampling and discovered cashews mixed in with the pecans. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.

So this appears to be an improper line cleanout, but could as well be an issue with in-process product or an even with addition where the wrong product was dumped.  Regardless, although both are nut products, they are different allergens and must be controlled as  such.

Product was distributed to 25 retail stores located in Connecticut, New York, New Jersey, New Hampshire, Pennsylvania, Ohio, Nevada, Florida, and Wisconsin.  Product was also sold online.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nats-nuts-issues-allergy-alert-potential-undeclared-cashews-nats-nuts-brand-cinnamon-whiskey-pecans
Nat’s Nuts Issues Allergy Alert on Potential Undeclared Cashews in Nat’s Nuts Brand Cinnamon Whiskey Pecans
Summary
Company Announcement Date:  October 17, 2025
FDA Publish Date:  October 17, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared cashews
Company Name:  Nat’s Nuts
Brand Name:  Nat’s Nuts
Product Description:  Cinnamon Whiskey Pecans

Florida Firm Recalls Ice Cream with Mismatched Lid and Carton Resulting In Undeclared Allergen

Publix, Lakeland, FL, has initiated a voluntary recall on one lot of Publix Rich & Creamy Vanilla Ice Cream, UPC 41415 03043, that may contain an undeclared egg allergen.  The Publix Rich & Creamy Vanilla Ice Cream half gallon container with a sell by date of “June 19, 2026 A” may contain Publix Rich & Creamy French Vanilla Ice Cream with a mismatch French Vanilla container lid.

Here is another instance of a mis-match between the lid and the container.  As part of an Allergen Preventive Control, there would need to be controls to ensure the carton matches the lid which matches the product.

The product was distributed to stores located in Alabama, Georgia, Kentucky, South Carolina, Tennessee and Florida, except for stores in Jacksonville, Tallahassee, Tampa and Sarasota.  There have been no reported cases of illness to date.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/publix-rich-creamy-vanilla-ice-cream-voluntarily-recalled-select-areas
Publix Rich & Creamy Vanilla Ice Cream Voluntarily Recalled in Select Areas
Summary
Company Announcement Date:  October 14, 2025
FDA Publish Date:  October 17, 2025
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared egg allergen
Company Name:  Publix
Brand Name:  Publix
Product Description:  Rich & Creamy Vanilla Ice Cream

Cheddar Popcorn Recalled Due to Undeclared Peanuts - The Risk of Licensing Brand Name

Jody’s Inc. of Norfolk, VA is recalling Cabot Creamery Sea Salt Caramel Cheddar Popcorn 6 oz (170 g) bag, lot number 2519907B1, Best If Enjoyed By: 07 15 26  due to presence of undeclared peanuts.  On October 15, 2025, the firm was notified by The Farmer Companies, Inc. that they received two customers complaints of peanuts found in their bags of the product.

In this case, Cabot Creamery licensed the use of its brand name to Jody's Inc, a popcorn company, through The Farmer Companies.   All good until the popcorn company fails to control allergens within their facility, resulting in a recall that impact the Cabot brand.  We are not told much beyond that, but it does bring up an important issue of co-branding and the need for the brand owner to ensure those that use that brand are top notch with regard to food safety and quality systems.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/jodys-inc-recalls-cabot-creamery-sea-salt-caramel-cheddar-popcorn-due-undeclared-peanuts
Jody’s Inc. Recalls Cabot Creamery Sea Salt Caramel Cheddar Popcorn Due to Undeclared Peanuts
Summary
Company Announcement Date:  October 17, 2025
FDA Publish Date:  October 17, 2025
Product Type:  Food & Beverages  
Reason for Announcement:  Due to presence of undeclared peanuts
Company Name:  Jody's Inc.
Brand Name:  Cabot Creamery
Product Description:  Sea Salt Caramel Cheddar Popcorn

WA Firm Recalls Frozen Shrimp Linked to FDA Advisory on Cesium in Indonesian Shipments

AquaStar (USA) Corp of Seattle, WA is voluntarily recalling a limited quantity of frozen shrimp imported from Indonesia because they may have been prepared, packed, or held under conditions whereby they may have become exposed to very low levels of cesium-137 (Cs-137).  This product is linked to the FDA Consumer Advisory issued in September for shrimp imported from Indonesia.  

Product was packed under the Best Yet, Waterfront Bistro, Aquastar, and Publix brand labels.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aquastar-usa-corp-recalls-shrimp-because-possible-health-risk
Aquastar (USA) Corp Recalls Shrimp Because of Possible Health Risk
Summary
Company Announcement Date:  October 17, 2025
FDA Publish Date:  October 17, 2025
Product Type:  Food & Beverages  Shellfish
Reason for Announcement:  Product may have been prepared, packed, or held under conditions whereby they may have become exposed to very low levels of cesium-137 (Cs-137)
Company Name:  AquaStar Corp
Brand Name:  AquaStar, Best Yet, Waterfront Bistro, Publix
Product Description:  Frozen Raw Shrimp

TX Firm Recalls Eggs After Salmonella Found in Processing Environment

Kenz Henz of Santa Fe, TX, is recalling its 12 count packages of "Grade AA Large Pasture Raised eggs" because they have the potential to be contaminated with Salmonella.  This comes after FDA inspected a processing facility and through environmental sampling, found extensive Salmonella contamination.

Current update as of September 29, 2025: FDA initiated an inspection at Black Sheep Egg Company’s egg processing facility and collected environmental samples. Of the samples collected, 40 environmental samples were positive for Salmonella including seven different strains of Salmonella. Some of these strains are known to cause human illness. FDA does not have information available at this time to suggest that this firm is the source of an ongoing outbreak.

No illnesses have been reported to date in connection with this problem.

The recalled "12 Count Pasture Raised eggs" in retail stores in Houston, TX.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kenz-henz-recalls-pastured-raised-eggs-because-possible-health-risk
Kenz Henz Recalls "Pastured Raised Eggs" Because of Possible Health Risk
Summary
Company Announcement Date:  October 16, 2025
FDA Publish Date:  October 17, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential to be contaminated with Salmonella
Company Name:  Kenz Henz
Brand Name:  Kenz Henz
Product Description:  Grade AA Large Pasture Raised Eggs

Health Warning Issued for Ready-To-Eat Meals Containing Riced Cauliflower That May Be Contaminated With Listeria

USDA-FSIS is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm containing a Food and Drug Administration (FDA) regulated ingredient, specifically riced cauliflower, that may be contaminated with Listeria monocytogenes (Lm).  The problem was discovered when FreshRealm notified FSIS that the riced cauliflower used in these products tested positive for Listeria monocytogenes.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-ready-eat-meals-containing-riced-cauliflower-may-be
FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Riced Cauliflower That May Be Contaminated With Listeria

FSIS Announcement

WASHINGTON, Oct. 7, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm containing a Food and Drug Administration (FDA) regulated ingredient, specifically riced cauliflower, that may be contaminated with Listeria monocytogenes (Lm). Based on current evidence, the products included in this public health alert are not related to any ongoing outbreak investigations. A recall was not requested because the products are no longer available for purchase.

Rice Products Recalled Due to the Potential for Small Stones in Product

Ben's Original is initiating a voluntary recall in the United States on a limited number of Ben's Original Long Grain White, Whole Grain Brown, and Long Grain & Wild Ready Rice products due to the possible presence of small, naturally occurring stones originating from the rice farm.  This is an isolated issue limited to these batches— no other Ben's Original™ products are affected.

In commercial rice operations, stones are removed through specific equipment that separates based on density.  Generally this is done with the use of forced air that causes the lighter rice grains to be separated from heavier rocks.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bens-originaltm-issues-voluntary-recall-select-bens-original-long-grain-white-whole-grain-brown-and
Ben’s Original™ Issues Voluntary Recall of Select Ben's Original Long Grain White, Whole Grain Brown, and Long Grain & Wild Ready Rice Products Due to Possible Presence of Small Stones from Farm
Summary
Company Announcement Date:  October 10, 2025
FDA Publish Date:  October 14, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foreign Body Contaminant – Small Stones
Company Name:  Ben’s Original
Brand Name:  Ben’s Original

WI and MN Establishments Recall Frozen Pet Products After FDA Testing Finds Salmonella

FDA testing has found Salmonella in two different frozen pet products, one from a company in MN and another in WI.  Both companies have issued recalls.

Foodynamics, of Wales, WI, is voluntarily recalling specific lots of Raw Dog Barkery, BellePepper Cats, and Kanu Pets brand freeze dried pet treats because they have the potential to be contaminated with Salmonella.  The recall is the result of FDA sampling which revealed the presence of Salmonella. Foodynamics has ceased the production and distribution of the product while it works with the FDA to continue its investigation into what caused the problem.  The recalled products were shipped from Wisconsin via UPS to retailers in Wisconsin, New York, and Florida. A total of 7 packages were distributed to consumers in these areas.  Foodynamics successfully traced 100% of the product distribution within hours of the recall notice and has contacted all direct customers. No adverse health effects have been reported in pets or humans to date.

Raw Bistro Pet Fare, Cannon Falls, MN is voluntarily recalling two product sizes of its frozen beef dog food because they may be contaminated with Salmonella.  The potential for contamination was identified after an FDA-collected sample from a distributor tested positive for Salmonella. To date, no illness of pets or humans related to this lot has been reported.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foodynamics-recalls-raw-dog-barkery-bellepepper-cats-and-kanu-pets-brand-freeze-dried-pet-treats
Foodynamics Recalls Raw Dog Barkery, BellePepper Cats, and Kanu Pets Brand Freeze-Dried Pet Treats Because Of Possible Salmonella Contamination
Summary
Company Announcement Date:  October 09, 2025
FDA Publish Date:  October 09, 2025
Product Type:  Animal & Veterinary  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness – Salmonella
Company Name:  Foodynamics
Brand Name:  Foodynamics
Product Description:  Freeze Dried Pet Treats

Arizona Firm Recalls Pasta Salad Made with Pasta Linked to Listeria Outbreak

 Sprouts Farmers Market of Phoenix, AZ is recalling select lots of Smoked Mozzarella Pasta Salad sold from the deli service counter or Grab & Go section after being alerted by their supplier Fresh Creative Foods of potential Listeria monocytogenes contamination of the pasta within the pasta salad.  This is part of the ongoing investigation into the Listeria outbreak linked to ready-to-eat pasta produced by Nate's Fine Foods, Inc.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sprouts-farmers-market-recalling-smoked-mozzarella-pasta-salad-because-possible-health-risk

Sprouts Farmers Market is Recalling Smoked Mozzarella Pasta Salad Because of Possible Health Risk

Summary
Company Announcement Date:  October 08, 2025
FDA Publish Date:  October 09, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness – Listeria monocytogenes
Company Name:  Sprouts Farmers Market
Brand Name:  Sprouts
Product Description:  Smoked Mozzarella Pasta Salad

WA Firm Recalls Vegetable Egg Rolls That May Contain Shrimp Rolls

Tai Foong USA of Seattle, Washington is recalling a limited quantity of Fusia Asian Inspirations Veggie Spring Rolls, net wt. 10oz, because the product may contain shrimp.  The recall was initiated after it was discovered that certain cases of Shrimp Spring Rolls may have been inadvertently packaged in boxes labeled as Vegetable Spring Rolls. The cause of this labeling error is being investigated. 

The affected Veggie Spring Rolls were distributed exclusively to ALDI stores nationwide and sold under the Fusia Asian Inspirations brand.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tai-foong-usa-issues-allergy-alert-undeclared-shrimp-fusia-asian-inspirations-veggie-spring-rolls
Tai Foong USA Issues Allergy Alert on Undeclared Shrimp in Fusia Asian Inspirations Veggie Spring Rolls
Summary
Company Announcement Date:  October 08, 2025
FDA Publish Date:  October 08, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared shrimp allergen
Company Name:  TAI FOONG USA
Brand Name:  Fusia Asian Inspirations
Product Description:  Veggie Spring Rolls

CA Firm Recalls Ground Cinnamon After FDA Finds Lead Contamination

Eureka Inc of Pomona, CA (10/6/2025) is recalling Durra Ground Cinnamon 100 gram plastic container because it has the potential to be contaminated with lead.  The recall was initiated after the FDA collected product samples and detected elevated levels of lead. The firm’s investigation is ongoing, including testing raw materials used in manufacturing the product


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/durra-ground-cinnamon-100-g-because-possible-health-risk
Durra Ground Cinnamon 100 G Because of Possible Health Risk
Summary
Company Announcement Date:  October 06, 2025
FDA Publish Date:  October 07, 2025
Product Type:  Food & Beverages  Spices, Flavors & Salts  
Reason for Announcement: Potential Metal Contaminant - Lead
Company Name: Eureka Inc.
Brand Name: Durra
Product Description:  Ground cinnamon

MN Firm Recalls Frozen Spinach After Listeria Positive Found in Supplier Bulk Case

Sno Pac Foods of Caledonia, MN, is recalling Del Mar 35 LB Bulk Organic Frozen Spinach and Sno Pac10 oz Organic Frozen Cut Spinach because they have the potential to be contaminated with Listeria monocytogenes.  This recall has been initiated due to possible Listeria monocytogenes. A bulk case of spinach from our supplier was tested and found positive for Listeria monocytogenes and was of the same lot code we used to repack the Sno Pac Organic Frozen Cut Spinach into 10 oz packages.

In this case, the spinach supplier is blanching, freezing, and bulk packing spinach.  The spinach supplier is the one controlling this hazard through incorporating a Sanitation Preventive Control(s) to prevent contamination after blanching through bulk packing.  Companies buying this spinach need to recognize Listeria as a hazard being controlled by the supplier, and implement a Supply Chain Preventive Control for this product from this supplier.  What would the Supply Chain Preventive Control entail?  Among many potential forms of verification, some would/could include verifying that the supplier has a Sanitation Preventive Control in place, obtaining a third-party audit or conducting an audit on that supplier, requesting testing results, and sampling and testing the incoming material.

The recalled Frozen spinach was distributed nationwide in retail stores and through distributors.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sno-pac-foods-recalls-del-mar-35-lb-bulk-frozen-spinach-and-10-oz-organic-frozen-cut-spinach
Sno Pac Foods Recalls Del Mar 35 LB Bulk Frozen Spinach and 10 oz Organic Frozen Cut Spinach
Summary
Company Announcement Date:  October 06, 2025
FDA Publish Date:  October 07, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential to be contaminated with Listeria monocytogenes
Company Name:  Sno Pac Foods, Inc.
Brand Name:  Sno Pac/Del Mar
Product Description:  Frozen Spinach

USDA Issues Health Alert for Home Delivered Meal Where Spinach Ingredient Positive for Listeria

USDA-FSIS is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm under the Hello Fresh brand containing spinach (FDA regulated ingredient) that may be contaminated with Listeria monocytogenes.  The problem was discovered when FreshRealm notified FSIS that the spinach used in these products tested positive for Listeria monocytogenes.

Here is another heat and serve (ready-to-eat) product that has a Listeria issue.  One ingredient, spinach, was found to be positive for Listeria.  Was this spinach pre-cooked (blanched) by the supplier or by cooked or partially cooked by FreshRealm (where it would been received raw and then cooked in the development of the meal)?  In either case, the company making the meal is responsible for ensuring the RTE meal is free from Listeria.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-ready-eat-meals-containing-spinach-may-be
FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Spinach That May Be Contaminated With Listeria

FreshRealm, Indianapolis, IN

FSIS Announcement

WASHINGTON, Oct. 6, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm containing a Food and Drug Administration (FDA) regulated ingredient, specifically spinach, that may be contaminated with Listeria monocytogenes (Lm).

FDA Issues Update on Listeria Outbreak Linked to Ready-to-Eat Pasta

FDA issued an update on the Listeria outbreak linked to ready-to-eat pasta produced by Nate's Fine Foods, Inc.  A number of recalls have been issued by various retailer nationwide.

To date, there have been 20 reported cases with 19 hospitalizations and 4 deaths.

Case Counts
Total Illnesses: 20
Hospitalizations: 19
Deaths: 4
Last Illness Onset: September 11, 2025
States with Cases: CA, FL, IL, IN, LA, MI, MN, MO, NC, NV, OH, SC, TX, UT, VA
Product Distribution: Nationwide

Interesting is that this has not received the same attention as the Listeria outbreak linked to Boar's Head product.  Granted, there were more cases and deaths, but any death from eating contaminated food is tragic.

FDA Outbreak Investigation
https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-listeria-monocytogenes-prepared-pasta-meals-june-2025
Outbreak Investigation of Listeria monocytogenes: Prepared Pasta Meals (June 2025)

Do not eat or serve certain meals containing pre-cooked pasta. FDA’s investigation is ongoing.

FDA Tightens Import Controls for Indonesia After Cesium Positive Testing for Shrimp and Now Cloves

After detecting ceseum 137 in a load of shrimp (which resulted in recalls for shrimp from the Indonesian supplier., PT. Bahari Makmur Sejati ) and then detecting the presence of Cs-137 in one sample of cloves from PT Natural Java Spice, the FDA issued an import alert for chemical contamination. Products from PT. Bahari Makmur Sejati and from PT Natural Java Spice and these companies will not be permitted to enter the U.S. market until these firms provide the FDA with information to adequately demonstrate that they have resolved the conditions that gave rise to the appearance of the violations.

Effective October 31, 2025, the agency will require import certification for shrimp and spices from certain regions of Indonesia, based on the risk of potential contamination of the food with Cesium-137.

"At this time, no product that has tested positive or alerted for Cs-137 has entered U.S. commerce. Currently, the FDA has identified that all implicated product is tied to PT. Bahari Makmur Sejati and PT Natural Java Spice, both firms of Indonesia."


https://www.fda.gov/food/environmental-contaminants-food/fda-response-imported-foods-potentially-contaminated-cesium-137
FDA Response to Imported Foods Potentially Contaminated with Cesium-137

CA Establishment Issues Recall for Corn Dogs for Foreign Wood Material in Batter

Foster Poultry Farms, LLC, a Livingston, Calif. establishment, is recalling approximately 3,843,040 pounds of chicken corn dog products that may be contaminated with extraneous material, specifically pieces of wood embedded in the batter.  The problem was discovered after FSIS received a consumer complaint involving an injury from consumption of these products. Additionally, the establishment received multiple consumer complaints, 5 of which involved injuries. 

On September 27, the Hillshire Brands Company, a Haltom City, Tex. establishment, recalled  approximately 58,000,000 pounds of corn dog and sausage on a stick products that may be contaminated with extraneous material, specifically pieces of wood embedded in the batter.   

These two recalls are probably related, but not clear how.

https://www.fsis.usda.gov/recalls-alerts/foster-poultry-farms-llc-recalls-chicken-corn-dog-products-due-possible-extraneous
Foster Poultry Farms, LLC Recalls Chicken Corn Dog Products Due To Possible Extraneous Matter Contamination

FSIS Announcement

WASHINGTON, Oct. 4, 2025 – Foster Poultry Farms, LLC, a Livingston, Calif. establishment, is recalling approximately 3,843,040 pounds of chicken corn dog products that may be contaminated with extraneous material, specifically pieces of wood embedded in the batter, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

NY Firm Recalls Noodles Due to Packaging Mix-Up Resulting in Undeclared Egg Allergen

Twin Marquis LLC is voluntarily recalling one production date of individually wrapped Twin Marquis® Thick Shanghai Style Plain Noodle packages due to possible undeclared egg allergen. The affected packages of Shanghai Style noodles, which do not list egg as an ingredient, may mistakenly contain Lo Mein noodles, which are made with egg.  The item being recalled was produced on May 20, 2025, at the company’s production facility in Brooklyn, New York. The company discovered the issue as the result of a complaint from a distributor.

The affected noodles were distributed through ethnic retail outlets nationwide.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/twin-marquis-llc-voluntarily-recalls-twin-marquisr-thick-shanghai-style-plain-noodle-packages-due
Twin Marquis LLC Voluntarily Recalls Twin Marquis® Thick Shanghai Style Plain Noodle Packages Due to Undeclared Egg
Summary
Company Announcement Date:  October 03, 2025
FDA Publish Date:  October 04, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential or Undeclared Allergen - Egg
Company Name:  Twin Marquis LLC
Brand Name:  Twin Marquis
Product Description:  Thick Shanghai Style Plain Noodles

Michigan Firm Recalls Dog Chews After FDA Testing Finds Salmonella

Best Buy Bones, Inc. of Mount Morris, Michigan is recalling four lots of Nature’s Own Pet Chews Bully Bites 1 Pound pet treats in 16 oz. bags with a shared expiration date of September 2027 because it has the potential to be contaminated with Salmonella.  The health risk was discovered when samples of the product were collected on September 11, 2025, and tested by the Food and Drug Administration. The product tested positive for Salmonella. The company has ceased production and distribution of this product as the FDA, and the company continue their investigation into what caused the problem.

34 bags of Nature’s Own Pet Chews Bully Bites 1 Pound pet treats were distributed out of Minnesota and sold through retail stores in Wisconsin after September 23.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/best-buy-bones-inc-recalls-natures-own-pet-chews-bully-bites-because-possible-salmonella-health-risk
Best Buy Bones, Inc. Recalls Nature’s Own Pet Chews Bully Bites Because of Possible Salmonella Health Risk
Summary
Company Announcement Date:  October 03, 2025
FDA Publish Date:  October 03, 2025
Product Type:  Animal & Veterinary Food & Beverages
Reason for Announcement: Potential Foodborne illness - Salmonella
Company Name:  Best Buy Bones, Inc.
Brand Name:  Nature’s Own
Product Description:  Pet Chews Bully Bites Treats

More Retailers Issue Recalls for Pasta Products Using Pasta Linked to Listeria Outbreak

More recalls were issued by various retailers for pasta product containing the pasta form Nate's Fine Foods that has been linked to a Listeria outbreak.

• Albertsons Companies updated their previously issued recall for product from Fresh Creative Foods, a division of Reser’s Fine Foods, Inc.
• Giant Eagle issued a recall for Smoked Mozzarella Pasta Salad
• Kroger Co. (NYSE: KR), recalled Basil Pesto Bowtie Salad and Smoked Mozzarella Penne Salad 

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/update-albertsons-companies-voluntarily-recalls-select-store-made-deli-items-containing-bowtie-pasta
UPDATE - Albertsons Companies Voluntarily Recalls Select Store-Made Deli Items Containing Bowtie Pasta Supplied by Fresh Creative Foods Due to an Ingredient Recall for Possible Listeria monocytogenes Contamination
Summary
Company Announcement Date:  October 01, 2025
FDA Publish Date:  October 02, 2025
Product Type:  Food & Beverages
Reason for Announcement:
Possible Listeria monocytogenes contamination  

Company Name:  Albertsons Companies
Brand Name:  Multiple brand names
Product Description:  Bowtie Pasta Salads and Meals

NY Distributor Recalling Enoki Mushrooms After State Testing Finds Listeria

New Age International Inc of Brooklyn, NY 11206 is recalling its 200g (7.05OZ) packaged of Signature Enoki Mushroom, Product of K Food (Korea Food Signature) because they may be contaminated with Listeria monocytogenes.  The contamination was discovered after sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of Listeria monocytogenes in some 200g packages of Signature Enoki Mushroom.

The recalled Signature Enoki Mushrooms were distributed to a retail store and distributor in New York City.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/new-age-international-recalls-signature-enoki-mushrooms-due-potential-health-risk
New Age International Recalls Signature Enoki Mushrooms Due to Potential Health Risk
Summary
Company Announcement Date:  September 29, 2025
FDA Publish Date:  October 01, 2025
Product Type:  Food & Beverages  
Reason for Announcement:  Product may be contaminated with Listeria monocytogenes
Company Name:  New Age International Inc
Brand Name:  Signature
Product Description:  Enoki Mushrooms

CA Bakery Recalls Bundt Cakes Due to Undeclared Wheat and Milk

Doan’s Bakery of Woodland Hills, CA is recalling White Chocolate Coconut and Carrot Bundt Cakes because they may contain undeclared wheat and milk.   This issue was discovered during a routine facility inspection on September 24, 2025. Doan’s Bakery took immediate corrective action, and updated labeling is now in place across all affected products.

The recalled bundt cakes were sold by Doan’s Bakery and distributed nationwide via mail order via goldbelly.com from June 1, 2025 through September 24, 2025.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/doans-bakery-issues-allergy-update-undeclared-wheat-and-milk-allergens-bundt-cakes
Doan’s Bakery Issues Allergy Update on Undeclared Wheat and Milk Allergens in Bundt Cakes
Summary
Company Announcement Date:  October 01, 2025
FDA Publish Date:  October 01, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared allergens, wheat and milk
Company Name:  Doan's Bakery
Brand Name: Doan's Bakery
Product Description:  White Chocolate Coconut & Carrot Bundt Cakes

Food Distributor Issues a Recall for Shrimp Pasta Product

Demers Food Group recalled select Scott & Jon's Shrimp Scampi with Linguini because the pasta is linked to the  recall by Nate’s Fine Foods of Roseville, CA.  This supplier's pasta has been linked to the Listeria outbreak reported in September.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/demers-food-group-voluntarily-recalls-select-scott-jons-shrimp-scampi-linguini-bowls-due-ingredient
Demers Food Group Voluntarily Recalls Select Scott & Jon's Shrimp Scampi with Linguini Bowls Due to an Ingredient Recall Initiated by Nate’s Fine Foods for Possible Listeria Monocytogenes Contamination
Summary
Company Announcement Date:  October 01, 2025
FDA Publish Date:  October 02, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential Listeria monocytogenes contamination.
Company Name:  Demers Food Group
Brand Name:  Scott & Jon's
Product Description:  Shrimp Scampi with Linguini

More Frozen Indonesian Shrimp Recalled After Linked to Cesium Contamination Issue

Sea Port Products Corp of Kirkland, WA is voluntarily recalling a limited amount of Sea Port brand bagged Frozen Raw Easy Peel White Shrimp Jumbo size 16/20 count/lb because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with Cesium-137 (Cs-137).  This is linked to the FDA advisory on frozen shrimp from Indonesia.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sea-port-products-corp-recalling-raw-frozen-easy-peel-white-shrimp-because-product-may-have-become
Sea Port Products Corp is Recalling Raw Frozen Easy Peel White Shrimp Because Product May Have Become Contaminated with Cesium-137 (Cs-137)
Summary
Company Announcement Date: September 30, 2025
FDA Publish Date: October 01, 2025
Product Type: Food & Beverages
Reason for Announcement:  Product May Have Become Contaminated with Cesium-137 (Cs-137)
Company Name:  Sea Port Products Corp
Brand Name:  Sea Port
Product Description:  Raw Frozen Easy Peel White Shrimp Jumbo size 16/20
Company Announcement
Sea Port Products Corp of Kirkland, WA is voluntarily recalling a limited amount of Sea Port brand bagged Frozen Raw Easy Peel White Shrimp Jumbo size 16/20 count/lb because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with Cesium-137 (Cs-137).

Another Recall of Pasta Product Linked to CA Pasta Processor with Listeria Issue

Reser’s Fine Foods, Inc., Albertsons Companies has voluntarily recalled five store-made deli items, supplied by Fresh Creative Foods, due to possible Listeria monocytogenes contamination.  The recall was initiated because these products contain a recalled bowtie pasta ingredient manufactured by Nate’s Fine Foods of Roseville, CA.  This CA company has been linked to a Listeria Outbreak with 20 cases and 4 deaths.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/albertsons-companies-voluntarily-recalls-select-store-made-deli-items-containing-bowtie-pasta
Albertsons Companies Voluntarily Recalls Select Store-Made Deli Items Containing Bowtie Pasta Supplied by Fresh Creative Foods Due to an Ingredient Recall for Possible Listeria monocytogenes Contamination
Summary
Company Announcement Date:  September 29, 2025
FDA Publish Date:  September 30, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Possible Listeria monocytogenes contamination
Company Name:  Albertsons Companies
Brand Name:  Albertsons Companies
Product Description:  Bowtie Pasta Salads and Meals

MN Candy Company Recalls Chocolate Candy Product for Undeclared Cashews

Abdallah Candies is voluntarily recalling a specific lot of Pecan Caramel Clusters, due to a mislabeled allergen. Product contains Cashews that were not listed on the product label.  The recall was initiated after a guest who purchased the Pecan Caramel Clusters discovered the mislabeled cashew allergen.

Product was sold and distributed exclusively to Lunds & Byerlys, as a private label, sold in the state of Minnesota. 


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/abdallah-candies-issues-voluntary-recall-pecan-caramel-clusters-due-undeclared-mislabeled-allergens
Abdallah Candies Issues a Voluntary Recall of Pecan Caramel Clusters Due to Undeclared, Mislabeled Allergens
Summary
Company Announcement Date:  September 30, 2025
FDA Publish Date:  September 30, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Due to a mislabeled allergen, cashews
Company Name:  Abdallah Inc.
Brand Name:  Lunds & Byerlys
Product Description:  Chocolate candy with nuts.

CT Processor of RTE Produce Cited for Listeria Control Violations

FDA issued a Warning Letter to Gracie's Kitchens, Inc. of New Haven, CT, a  manufacturer of ready-to-eat (RTE) fresh cut fruits and vegetables, sauces, and non-RTE (NRTE) vegetable products. 

FDA "found serious violations of the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food regulation (CGMP & PC rule), Title 21, Code of Federal Regulations, Part 117 (21 CFR Part 117). Additionally, FDA collected environmental samples (i.e., swabs) from various areas in your processing facility. FDA laboratory analysis of the environmental swabs found the presence of Listeria monocytogenes (L. monocytogenes)" in the facility.

Lack of Listeria Control 

• As evidenced by recurring environmental findings of L. monocytogenes in the facility, the company did not implement sanitation controls adequate to ensure that the facility was maintained in a sanitary condition to significantly minimize or prevent the hazard of the environmental pathogen L. monocytogenes,
•  The positive swabs were recovered, while the facility was processing RTE vegetables and fruit, from food contact surfaces in the main production area, including:
• A cutting board on the surface of Table (b)(4) holding a tray of raw chicken on one side and packed potatoes on the other side.
• The interior of a grey bin next to Table (b)(4) holding artichokes in the process of being stuffed.
• Reoccurrence - This was not the first time that L. monocytogenes was found in environmental swabs collected in the facility. On April 9, 2024, FDA detected L. monocytogenes in (b)(4) environmental swab from the left side of the floor surface area in the cooler.
• In reviewing the facility’s environmental monitoring program, FDA noted that the company's own environmental monitoring program has repeatedly found L. monocytogenes and Listeria spp.  A review of the laboratory reports dated May 7, May 9, May 11, May 18, May 20, and May 22, 2024, found Listeria spp. was recovered from multiple non-food-contact surfaces, including but not limited to the concrete floor patch by table (b)(4) sampled on May 8, May 14, and May 16, 2024. On May 16, 2024, the concrete patch by table (b)(4) was also positive for L. monocytogenes.
• Not following the environmental monitoring procedure - the company did not perform any vector testing, intensified cleaning, and sanitizing, nor did it conduct additional activities to identify sources and routes of contamination. Furthermore, FDA's review of the laboratory reports found environmental swabs collected from the wheels on green cart (b)(4) on May 2, 2024, and green cart (b)(4) on May 8, 2024, were positive for Listeria spp. These carts move freely from the main processing area to other areas of the facility, including the cooler and loading dock. The company did not document this activity or any other follow-up activities. Retesting and vector testing were not conducted, and no other documentation was provided to show whether corrective actions were implemented.

Allergen Control 

• Failed to identify undeclared allergens due to incorrect labeling as a food safety hazard requiring a preventive control. The facility handles and manufactures stuffed vegetable products, including stuffed artichokes and stuffed mushrooms containing the following allergens: fish (pollack, whiting), wheat, sesame, crustacean shellfish (crab), egg, soy, and milk. Undeclared allergens are a known or reasonably foreseeable hazard.  
• Allergen preventive control program did not specify how sequencing will be accomplished or what safeguards will be in place to assure allergen ingredients are stored separately. The program does not contain written monitoring procedures including frequency, corrective actions, and verification procedures. Furthermore, there were no records documenting activities performed.

Supply Chain 

• The hazard analysis identifies biological hazards at the (b)(4) step as reasonably likely hazards to occur and identifies a supplier approval program, “(b)(4),” Rev 03/03/19 to control that hazard. Under the “(b)(4) section of your “(b)(4)” it states, “(b)(4).” The written procedure does not specifically require review of annual onsite audit results to ensure control of vegetative bacterial pathogens (e.g., Salmonella and L. monocytogenes) in raw materials or other ingredients via the supply-chain program.

GMP issues were observed, many of which can be real issues for the spread of Listeria within an operation.  These include:

• Rinsing tables (b)(4) where water routinely splashed off the walls on to the cutting tables (food contact surface). FDA isolated L. monocytogenes from a swab collected from the cutting board on table (b)(4), which was used in the processing of RTE peppers and onions and NRTE potatoes.
• Spraying the floors after cleaning,where water was splashing off the floor on to the legs and frame of the cutting board tables and misting on to the surface of the cutting boards. 
• Spraying the floor mats, where water was splashing off the mats, floor, and drain onto equipment, including but not limited to the Urschel chopper and finished product packaging that are used to package both RTE and NRTE finished products. The Urschel chopper was later used to process NRTE butternut squash.
• High pressure water hoses were routinely placed on the floor and employees conducting sanitation were observed handling these hoses that were touching the floor with their gloved hands. After handling the hoses, the employees touched food surfaces including cutting boards and the middle conveyor belt with their gloved hands. The employees did not change their gloves or wash their hands. 
• During cleaning of white totes, water was observed splashing off the floor on to the bin stands and metal racks. The bin stands are used to hold totes of RTE produce and the metal racks were used to hold trays of RTE products.
• The plant floor in the middle room, at the doorways, and inside the walk-in cooler area is rough with exposed concrete, and pooling water was observed. There was an apparent red visible liquid (appeared to be liquid from raw meat products) observed pooling on the floor at the doorway between the middle and main processing. This is a high foot traffic area with employees, pallet jacks, and rolling carts moving freely between the front to the rear (b)(4) dumpster area and walk-in cooler during processing of RTE vegetables and fruits.

FDA Warning Letter

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/gracies-kitchens-inc-701613-09032025
Gracie's Kitchens, Inc.
MARCS-CMS 701613 — September 03, 2025

Small CA Soy Bean Processor Issued Warning Letter with Multiple Violations

FDA issued a Warning Letter to Tan Nam Corporation, a producer of ready-to-eat (RTE) and ready-to-drink (RTD) soybean products facility, located in Rosemead, CA .   This is a very small company, that would be considered  Qualified in terms of compliance (they do not need a formalized Food Safety Plan, but still have to have the necessary controls in place for safety).

It seems that this was more of a restaurant operation that was distributing product.   Because they were distributing, the first thing they need to do, but failed, was registering their facility.  Then they would file an attestation with FDA regarding their 'qualified' status.  That did not occur either.

What follows in the report is a laundry list of GMP violations, any of which could result in signification food safety issues.  Everything from lack of temperature control throughout the process to bad sanitation.

It is easy to overlook these small operations, but the same rules of food safety apply regardless of size.

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/tan-nam-corporation-708292-08252025
Tan Nam Corporation
MARCS-CMS 708292 — August 25, 2025

Importers Continue to Fail to Meet FSVP Requirements

Here are two recent examples of food importers who were cited for not addressing FSVP requirements for the food products that they import.

Ever Rich Foods LLC, Edison, NJ, did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR part 1.502(a) for any of the foods the company imports including:

• Sweet Kala Jamoon from the foreign supplier (b)(4) located in (b)(4).
• Kaju Pista Roll – Sweets from the foreign supplier (b)(4) located in (b)(4).
• Motichoor Ladoo from the foreign supplier (b)(4) located in (b)(4).

Delicias Del Country USA Inc Laredo, TX did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR part 1.502(a). Specifically, you did not develop an FSVP for any of the foods you import including the following foods:

• Sweet Kala Jamoon from the foreign supplier (b)(4) located in (b)(4).
• Kaju Pista Roll – Sweets from the foreign supplier (b)(4) located in (b)(4).
• Motichoor Ladoo from the foreign supplier (b)(4) located in (b)(4).

FDA Warning Letters
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/delicias-del-country-usa-inc-709970-07162025
Ever Rich Foods LLC
MARCS-CMS 715321 — September 12, 2025

FDA Warning Letter to Company Selling THC Gummies Highlights Growing Concern

FDA issued a Warning Letter to a Florida company that sells THC Gummies.  FDA focused on those products containing Delta-8 THC, but this and other cannabinoids are not allowed for food use.

"We note that your firm sells food products that contain cannabinoids other than Delta-8 THC. We know of no basis to conclude that any use in food of a cannabinoid, plant derived or otherwise, would be safe and lawful. For some cannabinoids, such as Delta-8 THC, the available data raise serious concerns about potential harm. For other cannabinoids, there is little or no available information concerning the safety of their use in food. No cannabinoid, plant derived or otherwise, is approved for any use in food as a food additive. Moreover, we know of no basis to conclude that any intended use in food of any cannabinoid satisfies the criteria for eligibility for GRAS status.

There was not inspection, as it appears, but this was from information obtained from the company's internet site.

The "U.S. Food and Drug Administration (FDA) reviewed your website at the Internet address stnrcreations.com in March 2025 and determined that you take orders there for various human food products, which you represent as containing Delta-8 tetrahydrocannabinol (THC). FDA has determined that your products, STNR Delta-8 and Delta-9 Gummies in various flavors, STNR Delta-8 and Delta-9 Candy Clusters Nana Berry Gummies, STNR Delta-8 Gummies in various flavors, STNR Delta-8 and Delta-9 Cookies in various flavors, and STNR Delta-8 and Delta-9 Brownies in various flavors, are adulterated under section 402(a)(2)(C)(i) of the Federal Food, Drug, and Cosmetic Act (the Act), 21 U.S.C. § 342(a)(2)(C)(i), because they bear or contain an unsafe food additive. Furthermore, it is a prohibited act to introduce adulterated food into interstate commerce under section 301(a) of the Act, 21 U.S.C. § 331(a)."

FDA states that there is an increasing amount of companies selling such products, and it is a concern.

FDA has observed a proliferation of products containing the cannabinoid, Delta-8 THC, and has expressed serious concerns about products containing Delta-8 THC that include: 1) Delta-8 THC products have not been evaluated or approved by FDA for safe use and may be marketed in ways that put the public health at risk; 2) FDA has received adverse event reports involving Delta-8 THC containing products, including for your Delta-8 and Delta-9 Watermelon Lemonade product specifically; 3) Delta-8 THC has psychoactive and intoxicating effects; 4) FDA is concerned about the processes used to create the concentrations of Delta-8 THC claimed in the marketplace; and 5) FDA is concerned about Delta-8 THC products that may be consumed by children, as some packaging and labeling may appeal to children

So what is Delta-8 THC and how does it differ from what we normally consider THC from marijuana?  This was a nice summary article in Forbes (https://www.forbes.com/health/cbd/delta-8-vs-delta-9/)

"Delta-8 THC is a naturally-occurring cannabinoid (a type of chemical in marijuana) in the cannabis sativa plant. However, as delta-8 typically occurs in relatively low quantities in the plant, the delta-8 found in retail CBD or cannabis products is often synthetically developed through a process of chemically converting CBD into delta-8.

Delta-8 and delta-9 THC produce similar psychoactive effects, but the effects from delta-8 are less potent. This is a result of the way delta-8 binds to the body’s endocannabinoid system (ECS), which regulates many functions in the central nervous system, including emotional and cognitive processing behavior, mood and more. Delta-8 binds to this system via a double bond structure in a particular carbon, which creates the psychoactive intoxicating effect, but to a lesser degree compared to delta-9.

“Delta-8 is a cannabinoid (cannabis-like molecule) that is very similar to the main active ingredient of regular cannabis, delta-9,” says Peter Grinspoon, M.D., a physician at Massachusetts General Hospital, instructor at Harvard Medical School, cannabis specialist and author of Seeing Through the Smoke: Cannabis: An Expert Doctor Untangles the Truth About Cannabis. “It functions by triggering our cannabinoid receptors in the same way that cannabis does.”

However, it’s worth noting that due to delta-8’s low natural presence in the cannabis sativa plant, artificially produced formulations of delta-8 may expose users to higher levels of the cannabinoid than they’d experience when using non-synthetic CBD. Additionally, commercially sold delta-8 and products containing delta-8 aren’t regulated by the U.S. Food and Drug Administration (FDA), meaning the chemical process by which the cannabinoids are made and the sanitary standard of the factories in which they’re made are also unregulated, potentially exposing users to unwanted risk and harm, according to the FDA."

FDA Warning Letters
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/stnr-creations-llc-698700-07162025

STNR Creations, LLC
MARCS-CMS 698700 — July 16, 2025

MN Produce Distributor Recalls Fresh Cut Cantaloupe After Testing Finds Listeria

Wholesale Produce Supply of Minneapolis, Minnesota is recalling fresh cut/processed cantaloupe, because it has the potential to be contaminated with Listeria monocytogenes.  The recall was the result of a routine sampling program by the company which revealed that the finished products potentially contained bacteria. Wholesale Produce Supply has suspended production and distribution of the affected lots as the company continues their investigation as to what caused the problem.  
No illnesses have been reported to date.

This indicates that the environmental sampling program found Listeria and the company has decided to recall product as part of their corrective action.

Fresh Cut Cantaloupe was sold to distributors in Nebraska, North Dakota and Wisconsin, who may have distributed into other states under the “Harvest Cuts” and “Fresh and Finest” brand at traditional grocery locations.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wholesale-produce-supply-minneapolis-minnesota-recalling-fresh-cutprocessed-cantaloupe-because-it
Wholesale Produce Supply of Minneapolis, Minnesota is Recalling Fresh Cut/Processed Cantaloupe, Because it has the Potential to be Contaminated With Listeria Monocytogenes
Summary
Company Announcement Date:  September 29, 2025
FDA Publish Date:  September 29, 2025
Product Type:  Food & Beverages  Fruit/Fruit Product
Reason for Announcement:  Potential to be contaminated with Listeria monocytogenes
Company Name:  Wholesale Produce Supply, LLC.
Brand Name:  Wholesale Produce Supply, LLC.
Product Description:  Fresh Cut Cantaloupe