Infant Botulism Outbreak Linked to Infant Formula - Source is Milk Powder However Root Cause Not Yet Determined

As of February 26, 2026, CDC declares that the botulism outbreak linked to infant formula is over. But the ultimate root cause beyond the organism's presence in the whole milk powder has not been determined.

"As of February 26, 2026, two isolates from one lot of organic whole milk powder, collected and analyzed by FDA, have been shown by whole genome sequencing (WGS) analysis to match a cluster of isolates reported by FDA on January 23, 2026. These two new isolates were collected by FDA at Dairy Farmers of America, the processor for Organic West Milk, which supplies ByHeart."

"The detection of Clostridium botulinum in infant formula, or ingredients, is complex. To date, WGS analysis has identified 17 different strains of this bacterium in samples from patients, finished products, and ingredients. While these sample results add to the available evidence needed to investigate the root cause of this outbreak, due to the complexities of Clostridium botulinum and limited scientific evidence currently available, FDA has not yet determined a root cause(s)."

Case Counts
Total Illnesses: 48
Confirmed cases: 28
Probable cases: 20
Hospitalizations: 48
Deaths: 0
Last Illness Onset: November 29, 2025
States with Cases: AZ, CA, ID, IL, KY, MA, MI, MN, NC, NJ, OR, PA, RI, TX, VA, WA, WI
Product Distribution: Online and nationwide (including Guam and Puerto Rico), and internationally

https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-infant-botulism-infant-formula-november-2025
Outbreak Investigation of Infant Botulism: Infant Formula (November 2025)
CDC declares this outbreak over. FDA’s investigation into the root cause is ongoing.

Gerber Recalls Biscuit Product After Flour Supplier Issues Recall for Foreign Material

Gerber Products Company is initiating a voluntary recall of limited batches of Gerber® Arrowroot Biscuits out of an abundance of caution due to the potential presence of soft plastic and/or paper pieces that should not be consumed. The material comes from an arrowroot flour supplier who initiated a recall. We are no longer working with the flour supplier.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gerber-products-company-announces-voluntary-recall-limited-batches-arrowroot-biscuits-out-abundance
Gerber Products Company Announces Voluntary Recall of Limited Batches of Arrowroot Biscuits Out of an Abundance of Caution Due to Potential Presence of Foreign Material Following Supplier Recall
Summary
Company Announcement Date:  January 26, 2026
FDA Publish Date:  January 28, 2026
Product Type:  Food & Beverages
Reason for Announcement:  potential presence of soft plastic and/or paper pieces
Company Name: Gerber Products Company
Brand Name: Gerber
Product Description:  Arrowroot biscuits

CA Importer Recalls Fish Ball Products for Undeclared Wheat and Sesame

Koikoi Trading Inc., Commerce, CA,  is recalling certain lots of FU ZHOU FISH BALL products in multiple pack sizes (200g, 400g, and 5LB) because the products may contain undeclared allergens: wheat and sesame.  The recall was initiated after it was discovered that product potentially containing wheat and sesame was distributed in packaging/labeling that did not declare the presence of these allergens in the ingredient statement and allergen declaration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/koikoi-trading-inc-issues-allergy-alert-undeclared-wheat-and-sesame-fu-zhou-fish-ball-200g-400g-5lb
Koikoi Trading Inc., Issues Allergy Alert on Undeclared Wheat and Sesame in FU ZHOU FISH BALL (200g / 400g / 5lb)
Summary
Company Announcement Date:  January 27, 2026
FDA Publish Date:  January 28, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared Allergen – Sesame, Wheat
Company Name:  Koikoi Trading Inc.
Brand Name:  Fu Zhou
Product Description:  Fish balls

CA Firm Recalls Packaged Imported Chia Seed After Supplier Recalls for Salmonella

Navitas Organics, Novato CA, is voluntarily recalling select lots of its 8oz Organic Chia Seeds due to possible Salmonella contamination. This recall is being conducted as a precautionary measure following a recall initiated by the company’s chia seed supplier.

Chia seeds are nutritionally beneficial for fiber, omega-3s, and antioxidants.  They will absorb water (up to 10 times their weight) forming a gelatinous texture when added into moist food matrix.  These seeds are often soaked for several hours to overnight into milk or similar to make a type of pudding.  So if Salmonella were present, this could provide opportunity for growth, or at the least, rehydration.

Product was distributed nationally through retail stores such as Whole Foods Market and online retailers including Amazon.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/navitas-organics-voluntarily-recalls-select-lots-8oz-organic-chia-seeds-because-possible-health-risk
Navitas Organics Voluntarily Recalls Select Lots of 8oz Organic Chia Seeds Because of Possible Health Risk
Summary
Company Announcement Date:  January 23, 2026
FDA Publish Date:  January 23, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness - Salmonella
Company Name:  Navitas Organics
Brand Name:  Navitas Organice
Product Description:  Organic Chia Seeds

FDA Issues Warning Letter to a Small California Pita Baking Company for GMP Violations

FDA issued a Warning Letter to Middle East Baking Co. a pita and bagel manufacturing facility located in Burlingame, CA .

The biggest issue was excessive insect activity, primary beetles, which were found throughout the facility.  There was also some rodent poop.  Along with this, as one would expect, was a lack of cleaning was also sited.  This resulting excessive food material buildup is what the beetles are feeding on.  There were some other GMP issues.  Surprisingly, not much mention of the post-processing area where post-process contamination seems like it could be a huge Salmonella risk.

Also of note,  this "facility meets the definition of a “qualified facility” under 21 CFR § 117.3; therefore, therefore not subject to having a food safety plan, and only "subject to the modified requirements in 21 CFR § 117.201 of the CGMP & PC rule.".

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/middle-eastsolis-baking-company-inc-dba-middle-east-baking-co-708017-07252025
Middle East/Soli's Baking Company, Inc. dba Middle East Baking Co.
MARCS-CMS 708017 — July 25, 2025

USDA Releases Pesticide Data Program Annual Summary

Each year, USDA-AMS releases its annual report on its Pesticide Data Program that summarizes data data on pesticide residues in food.  This report covers the data collected in 2024.

As seen in the past, data is generally good.  "In 2024, over 99 percent of the samples tested had residues below the tolerances established by the EPA with 42.3 percent having no detectable residue."   

And as seen in past years, domestic samples have less issues than imported.  "Residues exceeding the tolerance were detected in 0.77 percent (76 samples) of the total samples tested (9,872 samples). Of these 76 samples, 12 were domestic (15.8 percent), 63 were imported (82.9 percent), and 1 was of unknown origin (1.3 percent)." 

Where were the issues?  From page 23 and 24:

"Pesticides exceeding the tolerance were detected in 0.77 percent (76 samples) of the total samples tested (9,872 samples). Of these 76 PTV exceeder samples, 12 were domestic (15.8 percent), 63 were imported (82.9 percent), and 1 was of unknown origin (1.3 percent). PTV exceeder samples represented 0.2 percent of the total domestic  samples, 1.6 percent of the total imported samples, and 1.1 percent of unknown origin samples. The samples  containing pesticides that exceeded established tolerances included: 1 sample of avocados, 22 samples of fresh  blackberries, 8 samples of cherry tomatoes, 5 samples of cucumbers, 3 samples of fresh sweet corn, and 37 samples of tomatillos. Tomatillos accounted for 48.7 percent of all exceeder PTV samples in 2024. Commodities that did not have any samples exceeding the established tolerances were the following: almonds, apples, canned pumpkin, frozen blackberries, fresh/frozen pineapples, frozen sweet corn, head lettuce, leaf lettuce, onion, orange, potatoes, and salmon."

"Residues with no established tolerance were found in 3.7 percent (361 samples) of the total samples tested (9,872 samples). Of these 361 samples, 118 were domestic (32.7 percent), 230 were imported (63.7 percent), and 13 were of unknown origin (3.6 percent). PTV no-tolerance-established samples represented 2.0 percent of  the total domestic samples, 6.0 percent of the total imported samples, and 14.1 percent of the total unknown  origin samples. These samples included 356 fresh and processed fruit and vegetable samples and 5 almond samples. There were 337 samples that contained 1 pesticide for which no tolerance was established, 23 samples with 2 pesticides for which no tolerance was established, and 1 sample that contained 3 pesticides for which no tolerance was established. Fifty-eight of the 361 samples also contained 1 or more pesticides that exceeded an established tolerance. In most cases, the pesticides with no established tolerance were detected at low levels. Some pesticide residues may have resulted from unintentional spray drift in the field; planting of crops in fields previously treated with the pesticide; transfer of pesticide residues, postharvest fungicides, or other growth 

regulators applied to other commodities kept in the same storage facilities; or exposure to pesticides during transportation through the distribution chain. Commodities that did not have any samples with pesticides for which no tolerance was established were frozen sweet corn, oranges, potatoes, and salmon."

https://www.ams.usda.gov/sites/default/files/media/PDPAnnualSummary.pdf
Pesticide Data Program Annual Summary
Calendar Year 2024

Executive Summary

In 1991, the U.S. Department of Agriculture (USDA) Agricultural Marketing Service (AMS) was charged with designing and implementing the Pesticide Data Program (PDP) to collect data on pesticide residues in food, and Congress mandated the program in the 1996 Food Quality Protection Act (FQPA). PDP provides high-quality data on pesticide residues in food, particularly foods most likely consumed by infants and children. This 34th Pesticide Data Program summary presents results for samples collected in 2024.

Recall Reissued for Tuna with Bad Lids After Third Party Distributor Reships Product

A seafood company is reissuing a recall for product that was recalled in February and then accidently reshipped.

Tri-Union Seafoods is cautioning consumers that a third-party distributor inadvertently released quarantined product that was associated to a February 2025 recall. The initial voluntary recall was conducted following notification from our supplier that the “easy open” pull tab can lid on limited products had a manufacturing defect that may compromise the integrity of the product seal (especially over time), causing it to leak, or worse, be contaminated with clostridium botulinum, a potentially fatal form of food poisoning.  This current recall was initiated after Tri-Union Seafoods discovered that quarantined cases, associated with the initial recall, were inadvertently shipped by a third-party distributor. 

When recalled product is being held, there has to be tight controls in place so this type of thing, reshipping product, does not occur.  This can be especially a concern when third-party companies are the ones holding that product.  One could question why product from February with troublesome lids were still being held for close to a year later.  The longer something is not handled, the longer it sits, the greater the risk that it will escape.  This falls on the processor as much as the third party distributor.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tri-union-seafoods-identifies-additional-quantities-recalled-genovar-tuna-limited-retailers-due
Tri-Union Seafoods Identifies Additional Quantities of Recalled Genova® Tuna at Limited Retailers Due to Inadvertent Distribution of Previously Recalled Product
Summary
Company Announcement Date:  January 16, 2026
FDA Publish Date:  January 19, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential contamination with Clostridium botulinum
Company Name:  Tri-Union Seafoods
Brand Name:  Genova
Product Description:  Yellowfin Tuna

Georgia Establishment Recalls Frozen, Fully Cooked Chicken Breast After Lab Finds Listeria

Suzanna’s Kitchen, a Norcross, Ga., establishment, is recalling approximately 13,720 pounds of ready- to-eat grilled chicken breast fillet products that may be adulterated with Listeria monocytogenes.  The problem was discovered when a third-party laboratory sample reported a positive Listeria monocytogenes result in the ready-to-eat fully cooked grilled chicken breast fillets product.

The ready-to-eat grilled chicken breast fillet items were produced on October 14, 2025.   These  items (2 units of 5lb bags) were shipped to distribution centers for foodservice sales in Alabama, Florida, Georgia, Missouri, New Hampshire, North Carolina, and Ohio.

This is the type of situation that a robust environmental monitoring program is designed to prevent. Not only is USDA testing product, but so are customers, only done through outside contract laboratory services.  Unfortunately, the food establishment does not get to decide which outside laboratory a customer uses (if this is the case in this situation).

https://www.fsis.usda.gov/recalls-alerts/suzannas-kitchen-recalls-ready-eat-grilled-chicken-breast-fillet-products-due
Suzanna’s Kitchen Recalls Ready-To-Eat Grilled Chicken Breast Fillet Products due to Possible Listeria Contamination

FSIS Announcement

WASHINGTON, Jan. 16, 2026 – Suzanna’s Kitchen, a Norcross, Ga., establishment, is recalling approximately 13,720 pounds of ready- to-eat grilled chicken breast fillet products that may be adulterated with Listeria monocytogenes (Lm), the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

Super Greens Dietary Supplement Powder Recalled After Linked to Salmonella Outbreak

FDA and CDC are investigating illnesses in a multistate outbreak of Salmonella Typhimurium infections linked to Live it Up-brand Super Greens dietary supplement powder produced by Superfoods, Inc. doing business as (dba) Live it Up of New York, NY. There have been 45 cases with 12 hospitalizations to date.  The company is recalling all Live it Up-brand Super Greens dietary supplement powder, including original and wild berry flavors, with lots beginning with the letter "A" and all stick pack products within expirations dates from 08/2026 to 01/2028 

Case Counts
Total Illnesses: 45
Hospitalizations: 12
Deaths: 0
Last Illness Onset: December 30, 2025
States with Cases: AL, CT, DE, IA, IL, KY, MA, ME, MI, MN, MO, NE, NY, OH, PA, SC, TN, UT, VT, WA, WI
Product Distribution: Nationwide


https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-salmonella-dietary-supplement-january-2026
Outbreak Investigation of Salmonella: Dietary Supplement (January 2026)
Do not eat, sell or serve recalled Live it Up-brand Super Greens dietary supplement powder. FDA’s investigation is ongoing.
Product
All Live it Up-brand Super Greens dietary supplement powder, including original and wild berry flavors, with lots beginning with the letter "A" and all stick pack products within expirations dates from 08/2026 to 01/2028 have been recalled.

Cheese Recall Reposted a Month After It Was Issued

FDA is issuing a recall notice that was reissued last month regarding Ambriola Company's recall of select cheese products after routine testing confirmed the presence of Listeria monocytogenes. The recall was initially posted at the end of November, but it was reissued on December 3 to include additional product identification.  It seems that FDA did not post this at that time, and so are posting it now.  However, the main stream press is reporting this again which makes it seem as if it is a new recall.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ambriola-company-issues-recall-cheese-products-because-listeria-health-risk
The Ambriola Company Issues Recall of Cheese Products Because of Listeria Health Risk
Summary
Company Announcement Date:  December 03, 2025
FDA Publish Date:  January 15, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential to be contaminated with Listeria monocytogenes
Company Name:   The Ambriola Company
Brand Name:   Ambriola, Locatelli, Member’s Mark, Pinna, and Boar’s Head
Product Description:  Cheese

NY Firm Recalls Traditional Indian Sweets for Undeclared Milk

Karison Foods & Snacks Inc of Port Washington, NY 11050 is recalling 12 oz containers of ‘PANJIRI’, ‘ALSI PINNI’, ‘PUNJABI PINNI’, ‘BESAN LADDOO’, and ‘NO SUGAR ADDED BESAN LADDOO’ due to undeclared milk allergen.   During a routine inspection conducted at the firm, it was found that the milk allergen is undeclared on labels.

These items are traditionally made with ghee, a type of clarified butter.  This may be the case here that ghee was used.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/food-business-karison-foods-snacks-inc-recalls-panjiri-alsi-pinni-punjabi-pinni-besan-laddoo-and-no
Food Business Karison Foods & Snacks Inc Recalls ‘PANJIRI’, ‘ALSI PINNI’, ‘PUNJABI PINNI’, ‘BESAN LADDOO’, and ‘NO SUGAR ADDED BESAN LADDOO’ Due to Undeclared Milk Allergen
Summary
Company Announcement Date:  January 12, 2026
FDA Publish Date:  January 12, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential or Undeclared Allergen – Milk
Company Name:  Karison Foods & Snacks Inc
Brand Name:  Karison
Product Description:  Panjiri, pinni, and laddoo

California Firm Recall Sea Moss Gel for Improper Process Controls Resulting in Botulism Risk

Diva Fam Inc. ("Diva Fam" or the "Company") today (January 9, 2026) announced a voluntary recall of all lots and flavors of Sea Moss Gel Superfood due to lack of required regulatory authorization and temperature monitoring records for pH-controlled food products.  The matter was identified during a California Department of Public Health inspection that raised questions regarding regulatory authorization and related production records for certain distributed products. The Company is cooperating fully with regulatory authorities and has initiated this voluntary recall to ensure regulatory alignment.

The company is making a sea moss gel, which if not adjusted for pH after heating to set the gel, could become essentially a petri dish for growing organisms, specifically Clostridium botulinum.  


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/diva-fam-inc-announces-voluntary-recall-sea-moss-gel-superfood-products-due-possible-health-risk
Diva Fam Inc. Announces Voluntary Recall Of Sea Moss Gel Superfood Products Due to Possible Health Risk
Summary
Company Announcement Date:  January 09, 2026
FDA Publish Date:  January 12, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness - Botulism
Company Name:  Diva Fam Inc.
Brand Name:  True Sea Moss
Product Description:  Sea Moss Gel Superfood in various flavors (16 FL OZ glass jars)

Colorado Firm Recalls Bread Crumbs for Undeclared Allergens

VH Foods Inc. DBA Outside The Breadbox of Colorado Springs, CO is recalling its 8 ounce packages of "Bread Crumbs" because they may contain undeclared egg and milk.  The recall was initiated after it was discovered that the egg and milk product was distributed in packaging that did not reveal the presence of eggs or milk. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.  

One could guess that the wrong bread crumbs were added to the prelabeled package.  Here, proper labeling of in-process product and then selection of that product is so important.  Allergen Preventive Controls need to address these elements.    Note that the label does have the precautionary statement, but that does nothing to prevent this recall.

This was an isolated incident occurring on one production date.  The recalled "Bread Crumbs" were distributed in Colorado retail stores and through mail orders.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vh-foods-inc-dba-outside-breadbox-issues-allergy-alert-undeclared-egg-and-milk-bread-crumbs
VH Foods Inc. DBA Outside The Breadbox Issues Allergy Alert on Undeclared Egg and Milk in "Bread Crumbs"
Summary
Company Announcement Date:  January 12, 2026
FDA Publish Date:  January 12, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential or Undeclared Allergen – Egg and Milk
Company Name:  VH Foods Inc. DBA Outside The Breadbox
Brand Name:  Outside the Breadbox
Product Description:  Bread Crumbs

NC Firm Recalls Flavored Chocolate Bars After Contract Manufacturer Finds Salmonella in Product

Spring & Mulberry is voluntarily recalling various types of  flavored Chocolate Bar (2.1 oz) due to possible contamination with Salmonella.  The potential for contamination was first noted after routine third-party testing conducted by the company’s contract manufacturer revealed finished product tested positive for Salmonella.  The recall was initially for the Mint Leaf Date Sweetened Chocolate Bar (2.1 oz) but that recall was expanded five days later to include additional flavors.

There have been no confirmed illnesses or adverse health effects reported to date.  The affected products were available for purchase online and through select retail partners nationwide since September 15, 2025.

Food entrepreneurs who build a brand relying on co-manufacturers live and die by quality and food safety systems of that co-man.  I always recommend that someone from the organization take training to understand the technical elements of making safe quality product and then ensure that the co-mans are compliant.  With that, requiring co-mans to have 3rd party certification is a big part of that picture, but then reviewing the food safety plan with its preventive control elements to ensure the necessary elements have been determined and are being properly implemented. 


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/spring-mulberry-expands-voluntary-recall-select-chocolate-bars-due-possible-salmonella-contamination
Spring & Mulberry Expands Voluntary Recall of Select Chocolate Bars Due to Possible Salmonella Contamination
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/spring-mulberry-expands-voluntary-recall-select-chocolate-bars-due-possible-salmonella-contamination
Summary
Company Announcement Date:  January 14, 2026
FDA Publish Date:  January 15, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness - Salmonella
Company Name:  Spring & Mulberry
Brand Name:  Spring & Mulberry
Product Description:  Multiple Flavors of Chocolate Bars

NJ Distributor Recalls Shrimp Paste For Elevated Lead Levels Which Resulted in Injury

Gusto Group Inc. of Paterson, NJ is recalling [Klong Kone] Shrimp Paste (Klong Kone) '454 G. (1 LBS)' and ‘910 G. (2 LBS)’ because it has the potential to be contaminated with elevated levels of lead.

To date, there has been one report of four children becoming ill, which involved diarrhea and elevated blood levels. This recall was initiated following this report of illness associated with consumption of the product. The FDA collected product samples from retail locations and lab analysis found that the finished products contained elevated levels of lead. The company has ceased distribution of this lot. 

The recalled [Klong Kone] Shimp Paste (Klong Kone) “454 G. (1 LBS)” and “910 G. (2 LBS),” is packaged in a white plastic jar with a red cap was directly distributed to the two retailers listed below, located IA and NJ , between April 2023 to December 2023 There were no online sales


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gusto-group-inc-recalls-shrimp-paste-klong-kone-454-g-1-lbs-and-910-g-2-lbs-because-possible-health
Gusto Group Inc. Recalls Shrimp Paste (Klong Kone) ‘'454 G. (1 LBS)’ and ‘910 G. (2 LBS)’ because of Possible Health Risk
Summary
Company Announcement Date:  January 08, 2026
FDA Publish Date:  January 08, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential Metal Contaminant - Lead
Company Name:  Gusto Group Inc.
Brand Name:  Klong Kone
Product Description:  Klong Kone Shrimp Paste

Connecticut Facility Recalls Hummus Products Due to Undeclared Sesame

The Connecticut Department of Consumer Protection Food and Standards Division is warning the public that Carrot Top Country Kitchens LLC, DBA Carrot Top Kitchens of Bridgeport (formerly Redding), is recalling 5 varieties of hummus due to undeclared sesame.

The recalled products were distributed to Rochambeau Farm Store (Bedford, NY). The product has also been sold at farmers markets in Connecticut.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/carrot-top-kitchens-bridgeport-formerly-redding-issues-class-ii-recall-hummus-containing-undeclared
Carrot Top Kitchens of Bridgeport (formerly Redding) Issues a Class II Recall of Hummus Containing Undeclared Sesame
Summary
Company Announcement Date:  January 06, 2026
FDA Publish Date:  January 07, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential or Undeclared Allergen – Sesame
Company Name:  Carrot Top Kitchens
Brand Name:  Carrot Top Kitchens
Product Description:  Hummus Varieties

CA Company Expands Recall of Tamale Products Due to Improper Processing

Primavera Nueva Inc., Sonoma, CA, is expanding its recall of its 4-count tamales because of an undercooking process condition of the products resulting in the potential to be contaminated with Listeria monocytogenes. The expanded recall includes additional products.  The initial recall was posted on December 17, 2025.

The issue was that the products were sold as ready-to-heat, which is really ready-to-eat, but an ingredient used in the product had to be fully cooked first, but was not when the tamale product was made.  

"The products were made with a frozen ingredient labeled “Not Ready to Eat. Must Be Thoroughly Cooked Before Eating.” During an FDA inspection on October 10, 2025, the agency determined that earlier production records did not consistently verify internal cooking temperatures needed to control potential biological hazards, including Listeria monocytogenes".

So while Listeria was not actually detected in the product, it is a risk, as would other pathogens such as Salmonella.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/primavera-nueva-inc-issues-voluntary-recall-select-4-count-tamales-because-possible-health-risk-0
Primavera Nueva Inc. Issues Voluntary Recall of Select 4-Count Tamales Because of Possible Health Risk- Revised to Include Roasted Pumpkin & White Cheddar, a Seasonal Item
Summary
Company Announcement Date:  January 05, 2026
FDA Publish Date:  January 07, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Potential presence of Listeria monocytogenes
Company Name:  Primavera Nueva Inc.
Brand Name:  Primavera
Product Description:  Tamales

CA Importer Recalls Mustard Product Due to Undeclared Wheat

Newway Import Inc., located in La Puente, CA 91744, is recalling “Preserved Mustard in Soybean Oil” (Brand: Cai Hua Xiang) because the product may contain undeclared wheat.  The recalled product is Cai Hua Xiang brand preserved mustard in soybean oil.  The recall was initiated after it was discovered that the product contained wheat but was distributed in packaging that did not declare wheat as an allergen.

The ingredient statement includes soy sauce which usually contains wheat.  The wheat was not declared on the label.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/newway-import-inc-issues-allergy-alert-undeclared-wheat-preserved-mustard-soybean-oil-la-puente

Newway Import Inc. Issues Allergy Alert on Undeclared Wheat in “Preserved Mustard in Soybean Oil” La Puente, Calif. – December 23, 2025
Summary
Company Announcement Date:  December 23, 2025
FDA Publish Date:  January 05, 2026
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared wheat
Company Name:  Newway Import Inc.
Brand Name:  Newway Import
Product Description:  Preserved mustard in soybean oil

Warning Letter Issued to Feed Mill for Excessive Mycotoxins in Feed That Led to Animal Deaths

FDA issued a Warning Letter to King Farm, Dover, DE, a manufacturer of non-medicated animal food, after a series of deaths to horses and a goat promoted an FDA investigation. "This inspection was initiated after FDA became aware of at least 30 horse deaths and potentially one goat death after consuming your animal food products that were contaminated with the mycotoxin fumonisin."

FDA found levels ranging from 18 to 36 ppm in the feed, while the limit for horses is 5ppm.

Having excessive levels of the toxin in the feed, FDA identified that the company did not have any practices in place to prevent it. FDA stated the operation "did not have procedures in place, conduct routine testing, or have any processes in place to determine whether mycotoxins such as fumonisin, aflatoxin, or deoxynivalenol (DON/vomitoxin) are present at levels that can cause injury or illness to animals or humans in these grain and grain co-products you receive, store, and use in your animal food products."

In addition, the company "failed to report a reportable food to the Reportable Food Registry (RFR) within twenty-four hours of determining that it is a reportable food (i.e., an animal food for which there is a reasonable probability that the use of, or exposure to, such animal food will cause serious adverse health consequences or death to animals). Failure to submit a required reportable food report is a prohibited act."

What are fumonisins and what is allowed in feed (FDA https://www.fda.gov/regulatory-information/search-fda-guidance-documents/guidance-industry-fumonisin-levels-human-foods-and-animal-feeds)

Fumonisins are environmental toxins produced by the molds Fusarium moniliforme (F. verticillioides), F. proliferatum, and other Fusarium species that grow on agricultural commodities in the field or during storage. These mycotoxins have been found as contaminants worldwide, mainly in corn. More than ten types of fumonisins have been isolated and characterized. Of these, fumonisin B1 (FB1), fumonisin B2 (FB2), and fumonisin B3 (FB3) are the major fumonisins produced in nature. The most prevalent of these mycotoxins in contaminated corn is FB1, which is believed to be the most toxic (1, 2).

Occurrence in Raw Corn - The extent of contamination of raw corn with fumonisins varies with geographic location, agronomic and storage practices, and the vulnerability of the plants to fungal invasion during all phases of growth, storage, and processing. The levels of fumonisins in raw corn are also influenced by environmental factors such as temperature, humidity, and rainfall during pre-harvest and harvest periods (3). High levels of fumonisins are associated with hot and dry weather, followed by periods of high humidity. High levels of fumonisins may also occur in raw corn that has been damaged by insects (4, 5). Further, fumonisin levels in raw corn can increase under improper storage conditions. For example, optimal growth of fumonisin-producing molds that lead to increased levels of fumonisins in raw corn can occur when the moisture content of harvested raw corn during storage is 18-23 percent (5).

Animal Feeds

Corn and corn by-products intended for: Total Fumonisins (FB1+FB2+FB3)

Equids (horses) and rabbits 5 ppm  (no more than 20% of diet)**

Swine and catfish 20 ppm  (no more than 50% of diet)**

Breeding ruminants, breeding poultry and breeding mink* 30 ppm (no more than 50% of diet)**

Ruminants > 3 months old being raised for slaughter and mink being raised for pelt production 60 ppm  (no more than 50% of diet)**

Poultry being raised for slaughter 100 ppm  (no more than 50% of diet)**

All other species or classes of livestock and pet animals 10 ppm  

(no more than 50% of diet)**

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/king-farm-713276-12042025
WARNING LETTER

King Farm
MARCS-CMS 713276 — December 04, 2025

Idaho Establishment Recalls Raw Ground Beef After FSIS Testing Finds E. coli O26

Mountain West Food Group, LLC, a Heyburn, Idaho establishment, is recalling approximately 2,855 pounds of raw ground beef products that may be contaminated with E. coli O26.  The problem was discovered during routine FSIS testing and the sampling results showed the presence of E. coli O26.

"E. coli O26, like the more common E. coli O157:H7, is a serovar of Shiga toxin-producing E. coli (STEC). People can become ill from STECs 28 days (average of 34 days) after exposure to the organism.....The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart."

The product was shipped to distributors in California, Colorado, Idaho, Montana, Pennsylvania, and Washington for further distribution for retail sales.


https://www.fsis.usda.gov/recalls-alerts/mountain-west-food-group-llc-recalls-ground-beef-products-due-possible-e--coli-o26
Mountain West Food Group, LLC Recalls Ground Beef Products Due To Possible E. Coli O26 Contamination
Mountain West Food Group LLC
FSIS Announcement

WASHINGTON, Dec. 27, 2025 – Mountain West Food Group, LLC, a Heyburn, Idaho establishment, is recalling approximately 2,855 pounds of raw ground beef products that may be contaminated with E. coli O26, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

Iowa Distributor Recalls Pet Treats After Testing Finds Salmonella

Consumers Supply Distributing, LLC of Sioux City, Iowa is recalling 4 lb. bags of Country Vet Biscuits – Original Meaty Flavor and 4 lb. bags of Heartland Harvest Dog Biscuits – Meaty Flavor with Chicken because they have the potential to be contaminated with Salmonella.  The recall was the result of a routine sampling program by the FDA which revealed that the finished products contained the bacteria. The company has ceased the production and distribution of the lot number as FDA and the company continue their investigation as to what caused the problem.

The recalled products were sold through retail stores in Colorado, Iowa, Kansas, Missouri, Texas, Montana and Nebraska.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/consumers-supply-distributing-llc-recalls-country-vet-biscuits-dogs-due-possible-salmonella-health
Consumers Supply Distributing, LLC Recalls Country Vet Biscuits for Dogs Due to Possible Salmonella Health Risk
Summary
Company Announcement Date:  December 24, 2025
FDA Publish Date:  December 24, 2025
Product Type:  Animal & Veterinary  Food & Beverages  Pet Food
Reason for Announcement:   Potential to be contaminated with Salmonella
Company Name:  Consumers Supply Distributing, LLC
Brand Name:  Country Vet, Heartland Harvest
Product Description:  Dog Biscuits

Minnesota Firm Recalls Macadamia Nut Frozen Cookie Dough for Undeclared Peanuts

Gregory’s Foods, Inc. of Eagan, MN is recalling its 2-pound 8.5-ounce packages of "Bag Full of Cookies" White Chocolate Macadamia Nut frozen cookie dough because some units may contain undeclared Peanut. Frozen Monster Cookie Dough, which contains Peanut, may be packaged in a bag that is labeled as White Chocolate Macadamia Nut.  The recall was initiated after it was discovered that the peanut-containing product was distributed in packaging that did not reveal the presence of peanuts.  
The error was isolated to certain units in one day’s production and has been corrected.

The recalled "Bag full of Cookies" White Chocolate Macadamia Nut frozen cookie dough was distributed in Minnesota, Wisconsin, and Nebraska in retail grocery stores and through distribution centers.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gregorys-foods-issues-allergy-alert-undeclared-peanuts-bag-full-cookies-white-chocolate-macadamia
Gregory’s Foods Issues Allergy Alert on Undeclared Peanuts in "Bag Full of Cookies" White Chocolate Macadamia Nut Frozen Cookie Dough
Summary
Company Announcement Date:  December 23, 2025
FDA Publish Date:  December 23, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared peanuts
Company Name:  Gregory's Foods, Inc.
Brand Name:  Gregory's Foods
Product Description:  Bag Full of Cookies White Chocolate Macadamia Nut Frozen Cookie Dough

Minnesota Food Distributor Recalls Extensive List of Products After Being Found to Be Held Under Insanitary Conditions

Gold Star Distribution, Inc. (Gold Star or “the Company”), a food distribution company based in Minneapolis, MN, is recalling all FDA regulated products due to the presence of rodent and avian contamination at their Minnesota facility.  

"The U.S. Food and Drug Administration (FDA) determined that the facility was operating under insanitary conditions, including the presence of rodent excreta, rodent urine, and bird droppings in areas where medical devices, drugs, human food, pet food, and cosmetic products were held. These conditions create a significant risk that products held at the facility may have been contaminated with filth and harmful microorganisms. Products held under insanitary conditions may become contaminated through contact with contaminated surfaces or exposure to airborne particulates associated with animal waste. Exposure to contaminated products can pose serious health risks to consumers, including the potential for bacterial contamination, which may result in illness or infection, including Salmonella. There are numerous hazards associated with rodents including the potential presence of Salmonella."

There is an extensive list of products that include animal and veterinary products, cosmetics  dietary supplements, drugs, medical devices, food and beverages.  

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gold-star-distribution-inc-issues-recall-certain-fda-regulated-products-three-states-including-drugs
Gold Star Distribution Inc., Issues Recall of Certain FDA-Regulated Products in Three States Including Drugs, Devices, Cosmetics, Human Foods, and Pet Foods
Summary
Company Announcement Date:  December 26, 2025
FDA Publish Date:  December 26, 2025
Product Type:  Animal & Veterinary  Cosmetics  Dietary Supplements  Drugs  Food & Beverages
Medical Devices
Reason for Announcement:  Potential Salmonella contamination, presence of rodent and avian contamination and insanitary conditions during the storage process.
Company Name:  Gold Star Distribution, Inc.
Brand Name:  Multiple brand names
Product Description:  All FDA-regulated products held at facility including drugs, medical devices, cosmetics, dietary supplements, human food, and pet food
Company Announcement 

CT Firm Recalls Chocolate Bars for Undeclared Almonds Misidentified as Macadamia Nuts on Label

Willy Pete’s Chocolate Company LLC of Harwinton, CT is recalling their Almond Despair chocolate bar due to undeclared almonds in the label’s ingredient statement. The ingredient statement incorrectly identifies macadamia nuts as present in the product.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/recall-notice-willy-petes-chocolate-company-llc-harwinton-issues-recall-chocolate-bars-due-almonds
Recall Notice: Willy Pete’s Chocolate Company LLC of Harwinton Issues Recall of Chocolate Bars Due to Almonds Not Declared in Ingredient Statement
Summary
Company Announcement Date:  December 22, 2025
FDA Publish Date:  December 23, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential or Undeclared Allergen - Almond
Company Name:  Willy Pete’s Chocolate Company LLC
Brand Name:  Willy Pete’s Chocolates
Product Description:  Almond Despair chocolate bar

MD Firm Recalls Cookie Tins After Labeling Issue Results in Undeclared Allergens

Atwater’s of Baltimore, MD, is recalling 197 cookie tins because they contain cookies made with almond, pecan, and walnut allergens.  The recall was voluntarily initiated after it was discovered that the product containing almonds, pecans, and walnuts was distributed in packaging that did not reveal the presence of the nut allergen. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's labeling process.

The product was distributed from 12/13/2025 through 12/22/2025 in Baltimore, Towson, and Catonsville, MD, and it reached consumers through retail stores and was gifted to three wholesalers


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/atwaters-issues-allergy-alert-undeclared-tree-nut-allergen-cookie-tin-labels
Atwater’s Issues Allergy Alert on Undeclared Tree Nut Allergen on Cookie Tin Labels
Summary
Company Announcement Date:  December 22, 2025
FDA Publish Date:  December 23, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared tree nut allergens, almonds, pecans, and walnuts.
Company Name:  Atwater's
Brand Name:  Atwater's
Product Description:  Cookie tins

Illinois Firm Expands Recall of Confectionary Product for Undeclared Pecans Due to Mis-packaging

Silvestri Sweets Inc. of Geneva, IL is expanding its recall of  5-ounce bags of Choceur branded Holiday Barks because they may contain undeclared allergens.  The initial recall was posted in late November but was expanded to include additional lot numbers and “best by” dates not covered in the original recall.  This issue was the result of mis-packaging.  


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/silvestri-sweets-expands-voluntary-allergy-alert-undeclared-pecan-and-wheat-cookie-butter-holiday
Silvestri Sweets Expands Voluntary Allergy Alert on Undeclared Pecan and Wheat in Cookie Butter Holiday Bark and Pecan, Cranberry & Cinnamon Holiday Bark
Summary
Company Announcement Date:  December 22, 2025
FDA Publish Date:  December 23, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared pecans and wheat
Company Name:  Silvestri Sweet, Inc.
Brand Name:  Choceur
Product Description:  Holiday Bark

Michigan Firm Recalls Christmas Cookies without Allergen Labeling

Troemner Farm of Atlantic Mine, MI is recalling Troemner Family Farm branded 6 oz and 12 oz Pfeffernusse Cookies, because it may contain undeclared milk, wheat, and soy.  This missing labeling was revealed during routine inspections. Subsequent investigation indicates missing labels were a cause of human error.

Pfeffernusse cookies are traditional German Christmas cookies spiced with black pepper, cinnamon, cardamom, and other flavors.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/troemner-roemner-farm-issues-allergy-alert-undeclared-milk-wheat-and-soy-pfeffernusse-cookies
Troemner Roemner Farm Issues Allergy Alert on Undeclared Milk, Wheat, and Soy in Pfeffernusse Cookies
Summary
Company Announcement Date: December 22, 2025

FDA Publish Date:December 22, 2025

Product Type:  Food & Beverages
Reason for Announcement:  Undeclared milk, wheat, and soy allergens

Company Name: Troemner Farm

Brand Name: Troemner Family Farm

Product Description:  Pfeffernusse Cookies

FDA Issues Warning Letter to Florida Farm Operation Related to Salmonella Outbreak Linked to Cucumbers

FDA issued a Warning Letter to Bedner Growers, a farm operation in Boynton Beach, FL after inspection in response to o the 2024 multi-state outbreak of human infections with Salmonella Africana and Salmonella Braenderup linked to the firm's cucumbers.

"On April 2, 2025, FDA collected Sample 1148702 consisting of (b)(4) environmental swabs from your cucumber packing line. FDA analyzed Sample 1148702 and determined that (b)(4) of the (b)(4) swabs, representing food contact surfaces, were positive for Salmonella. Whole Genome Sequencing (WGS) analysis revealed that, as of May 7, 2025, (b)(4) isolates matched (b)(4) 2025 clinical isolates in the National Center for Biotechnology Information’s (NCBI) database that were uploaded April 25, 2025, or later. The same (b)(4) isolates from sample 1148702 were pathogens associated with illness in the 2025 multi-state outbreak investigation of human infections with Salmonella Montevideo described below."

"As part of FDA’s investigation, on May 15, 2025, FDA collected Sample 1298712, cucumbers determined to have been grown at your farm, from a distribution center in Pennsylvania. Salmonella was detected and WGS analysis determined that two isolates from this sample matched the Salmonella Montevideo outbreak strain. In addition, multiple other strains of Salmonella were detected which matched other isolates in the National Center for Biotechnology Information’s (NCBI) database, including isolates from the 2024 multistate outbreak of human infections with Salmonella Africana and Salmonella Braenderup, and an isolate from a 2024 cucumber sample collected by the Pennsylvania Department of Agriculture, which was also determined to have been grown at your farm."

"On May 16, 2025, FDA received your written response, describing corrective actions taken by your farm since April 14, 2025. We note that your written response lacked supporting details, or evidence of implementation, except for a letter from the University of Florida, dated May 12, 2025, which describes the 3rd party sampling effort that occurred at your farm on April 16, 2025."

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/bedner-growers-inc-706726-11172025
WARNING LETTER

Bedner Growers, Inc.
MARCS-CMS 706726 — November 17, 2025

Canada - Pizza with Pepperoni and Bacon Recalled After Linked to E.coli O26 Outbreak

General Mills Canada is recalling Pillsbury brand Pizza Pops Pepperoni + Bacon products after being linked to an outbreak of E. coli O26.

Not too much more information than that.

Canadian Food Inspection Agency 
https://recalls-rappels.canada.ca/en/alert-recall/certain-pillsbury-brand-pizza-pops-pepperoni-bacon-recalled-due-e-coli-o26
Food recall warning
Certain Pillsbury brand Pizza Pops Pepperoni + Bacon recalled due to E. coli O26

Canadian Establishment Recalls Quiche with Ham Product for No USDA Import Inspection

Maître Saladier Inc. in Quebec, Canada, is recalling approximately 6,000 pounds of Lorraine Quiche products containing pork [in the form of ham] that were not presented for import reinspection into the United States.  The problem was discovered during routine FSIS import surveillance activities. There have been no confirmed reports of illness due to consumption of these products. 


https://www.fsis.usda.gov/recalls-alerts/maitre-saladier-inc--recalls-lorraine-quiche-products-imported-without-benefit
Maître Saladier Inc. Recalls Lorraine Quiche Products Imported Without Benefit of Import Reinspection

FSIS Announcement

WASHINGTON, Dec. 19, 2025 – Maître Saladier Inc. in Quebec, Canada, is recalling approximately 6,000 pounds of Lorraine Quiche products containing pork that were not presented for import reinspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

Oregon Establishment Recalls Kielbasa Product After Complaint for Metal

Olympia Provisions, a Portland, Ore., establishment, is recalling approximately 1,930 pounds of ready-to-eat (RTE) holiday kielbasa sausages that may be contaminated with foreign material, specifically metal.  The problem was discovered after the establishment notified FSIS that it received a consumer complaint regarding metal found in the product. There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a healthcare provider.

This item was shipped to retail locations in California, Oregon, and Washington, and was available nationwide through online direct-to-consumer sales.                      


https://www.fsis.usda.gov/recalls-alerts/olympia-provisions-recalls-ready-eat-holiday-kielbasa-sausage-products-due-possible
Olympia Provisions Recalls Ready-to-Eat Holiday Kielbasa Sausage Products Due to Possible Foreign Matter Contamination

WASHINGTON, Dec. 19, 2025 – Olympia Provisions, a Portland, Ore., establishment, is recalling approximately 1,930 pounds of ready-to-eat (RTE) holiday kielbasa sausages that may be contaminated with foreign material, specifically metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

Washington Firm Recalls Almondmilk Chocolate Due to Undeclared Hazelnut

Fran’s Chocolates, Ltd. of Seattle, WA is recalling 112 units of Fran’s Pure Bar Almondmilk Chocolate 46% Madagascar Plant-Based, net wt. 1.1oz, because it contains undeclared hazelnut.  The company had received a report of one adverse allergic event related to the consumption of Fran’s Pure Bar Almondmilk Chocolate 46% Madagascar Plant-Based. 

The Fran’s Pure Bar Almondmilk Chocolate 46% Madagascar Plant-Based product was sold in four Fran’s Chocolates stores in Seattle, WA, and it was also sold online.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frans-chocolates-ltd-issues-allergy-alert-undeclared-hazelnuts-frans-pure-bar-almondmilk-chocolate

Fran’s Chocolates, LTD. Issues Allergy Alert on Undeclared Hazelnuts in Fran’s Pure Bar AlmondMilk Chocolate 46% Madagascar Plant-Based Product
Summary
Company Announcement Date:  December 20, 2025
FDA Publish Date:  December 20, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Contains undeclared hazelnut
Company Name:  Fran's
Brand Name:  Fran’s
Product Description:  Almondmilk Chocolate 46% Madagascar Plant-Based

MA Firm Recalls Yogurtish Type of Product Due to Undeclared Almond

PlantBased Innovations, of Leominster, MA, is recalling Higher Harvest by H-E-B Dairy-Free Coconut Yogurt, Strawberry flavor because the product may contain undeclared almond.  The recall was initiated after a customer complaint revealed that product containing almond was distributed in packaging that did not declare the presence of almond.

The recalled product was distributed to H-E-B and shipped on November 24, 2025, through H-E-B distribution centers and retail grocery stores in Texas.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/plantbased-innovations-issues-allergy-alert-undeclared-almond-h-e-b-dairy-free-coconut-yogurt
PlantBased Innovations Issues Allergy Alert on Undeclared Almond in H-E-B Dairy-Free Coconut Yogurt, Strawberry Flavor
Summary
Company Announcement Date:  December 19, 2025
FDA Publish Date:  December 19, 2025
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared almond
Company Name:  PlantBased Innovations
Brand Name:  Higher Harvest by H-E-B
Product Description:  Dairy-Free Coconut Yogurt, Strawberry flavor

Additional Recall Posted for Frozen Shrimp from Indonesia Due to Cesium-137

Direct Source Seafood LLC, Bellevue, WA, is recalling approximately 83,800 bags of frozen raw shrimp, imported from Indonesia, sold under the Market 32 and Waterfront Bistro brands because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with cesium-137 (Cs-137).

This recall is linked to the ongoing shrimp recalls for product from Indonesia where cesium 137 was identified as potential contaminant.  While this recall comes months after the last recall related to this cesium issue, there was no reason stated.  In the notice, it states, "The FDA is actively investigating reports of Cs-137 contamination in shipping containers and frozen shrimp products manufactured in Indonesia by PT. Bahari Makmur Sejati (doing business as BMS Foods). As noted in the FDA statement issued on 10/7/25: “At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. marketplace.”"

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/direct-source-seafood-llc-recalling-frozen-raw-shrimp-because-product-may-have-become-contaminated
Direct Source Seafood LLC is Recalling Frozen Raw Shrimp Because Product May Have Become Contaminated with Cesium-137 (Cs-137)
Summary
Company Announcement Date:  December 19, 2025
FDA Publish Date:  December 19, 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:  Direct Source Seafood LLC
Brand Name:  Market 32 and Waterfront Bistro
Product Description:  Frozen Raw Shrimp

Michigan Firm Recalls Cheddar Cheese Product After Finding Listeria in Product.

Boss Dairy Farms, Charlevoix, MI, is voluntarily recalling one retail lot of Charlevoix Cheese Company 8oz Mild Cheddar Cheese because it has the potential to be contaminated with Listeria monocytogenes.  The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in an 8oz block of mild cheddar.

It is important to note that this cheeses is made from pasteurized milk so the contamination would be more likely to be from post-process contamination from an environmental source (rather than from the raw milk ingredient).

Another issue is that the company is only recalling one lot of cheese.  As we have seen in many cases, an environmental contamination issue will often impact multiple lots....unless there is good reason why only one lot was impacted.

Product was distributed in Michigan only through retail stores.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/boss-dairy-farms-voluntarily-recalls-retail-mild-cheddar-cheese-because-possible-health-risk
Boss Dairy Farms Voluntarily Recalls Retail Mild Cheddar Cheese Because Of Possible Health Risk
Summary
Company Announcement Date:  December 17, 2025
FDA Publish Date:  December 18, 2025
Product Type:  Food & Beverages  Cheese/Cheese Product
Reason for Announcement:  Potential to be contaminated with Listeria monocytogenes.
Company Name:  Boss Dairy Farms
Brand Name:  Charlevoix Cheese Company
Product Description:  Milk Cheddar Cheese

PA Firm Recalls Rice Bowl Product with Incorrect Bottom Label Missing Allergens

A.S.K. Foods, LLC of Palmyra, PA is recalling select 32 oz. containers of Publix Rice & Pigeon Peas because it contains undeclared soy.   The recalled Publix Rice & Pigeon Peas was packaged in a plastic tray where the top label indicates Publix Rice & Pigeon Peas, Net Wt. 32 OZ (2 LB) 907, the bottom label has CAVATAPPI PASTA as the first ingredient and has a code on the lid of “5387-4”, “5387-5” or “5387-6”.

In this case, the bottom label was incorrect.  The top label, Rice and Pigeon Peas is correct.  The bottom label was for a pasta product.  While unsure whether the pic of the bottom label provided by FDA is the full bottom label, I can see there it would be difficult for the line operator to easily see if it is correct.  Regardless, an Allergen Preventive Controls in the form of procedures for ensuring proper labels is needed.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ask-foods-llc-issues-allergy-alert-undeclared-soy-publix-rice-pigeon-peas
A.S.K. Foods, LLC Issues Allergy Alert on Undeclared Soy in Publix Rice & Pigeon Peas
Summary
Company Announcement Date:  December 18, 2025
FDA Publish Date:  December 18, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Contains undeclared soy
Company Name:  A.S.K. Foods, LLC
Brand Name:  Publix
Product Description:  Publix Rice & Pigeon Peas

Another Widely Publicized Recall of Salad Dressing Misses Mark for Relevance to Consumers

Another recall news story that was published by all the news outlets, but no reporter looked into the facts.  Over the past 6 days or so (December 17, 2025 and after), news outlets have been reporting a giant recall of salad dressing from a California company due to foreign material in the form of plastic.   The news articles show pictures of retail store sized bottles and makes it seem as though this is the same item consumers buy.   Two problems - the recall was issued one month ago (11/6/25), and bigger yet, it was foodservice sized containers (gallon sized or bigger).  Therefore, this recall as published is not relevant for the consumer, especially at this time.

Costco did issue a recall related to this item, however it was for salad items made with that salad dressing on November 7, 2025.  (file:///C:/Users/mwb124/Downloads/PLEASEPOST11-7-25MemberLetter-CaesarDressingRecall-ServiceDeliItems.pdf)

We are seeing an increasing number of these poorly informed recall news stories.  Reporters are using the Enforcement Reports (this one is below) instead of the FDA recall notices that are publicly released and then they fail to read the information on the Enforcement Notice.  There is a reason why FDA does not issue a Public Recall Notice for this and reporters need to ask why

Why does this story get reported now?  It seems when FDA finally classifies the recall, it makes it seem recent.

Why is this not good?  We are bombarded with news stories on recalls.  People may become weary of all the recalls published and are likely not to take action.  Others may become hypervigilant, throwing away good food due to concern.  Overall, it makes it seem that our food is less safe than it really is.

CBS News
https://www.cbsnews.com/news/salad-dressing-recall-foreign-objects-fda-ventura-foods/

Salad dressings recalled in 27 U.S. states because they could contain "foreign objects"

By Megan Cerullo

December 17, 2025 / 6:11 PM EST / CBS News

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Ventura Foods is recalling thousands of cases of salad dressings sold at retailers including Costco and Publix because the condiments could contain "foreign objects," according to an alert from the Food and Drug Administration.

CA Processor Recalls Tamales for inadequate Heat Processing Step

Primavera Nueva Inc.,  Sonoma, CA, is voluntarily recalling certain lots of its 4-count tamales because the products have the potential to be contaminated with Listeria monocytogenes.  The products were made with a frozen ingredient labeled “Not Ready to Eat. Must Be Thoroughly Cooked Before Eating.” During an FDA inspection on October 10, 2025, the agency determined that earlier production records did not consistently verify internal cooking temperatures needed to control potential biological hazards, including Listeria monocytogenes.  Primavera Nueva has fully corrected the issue—enhanced cooking-temperature monitoring and verification have been in place since October 11, 2025.

This product has heating instructions, but not validated cooking instructions, so the processor is responsible for ensuring the safety of the product to control biological hazards.  If an ingredient is used where there is the potential to have a biological hazard, then a process control in the form of cooking is needed.  From this notice, it appears that the processor did not have a sufficiently validated heating step in place.

Product was distributed by Primavera Nueva Inc. in California and Nevada to retail stores

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/primavera-nueva-inc-issues-voluntary-recall-select-4-count-tamales-because-possible-health-risk

Primavera Nueva Inc. Issues Voluntary Recall of Select 4-Count Tamales Because of Possible Health Risk
Summary
Company Announcement Date:  December 17, 2025
FDA Publish Date:  December 17, 2025
Product Type:  Food & Beverages  Foodborne Illness  
Reason for Announcement:  Potential presence of Listeria monocytogenes.
Company Name:  Primavera Nueva Inc.
Brand Name:  No Brand
Product Description:  Tamales

Retailer Recalls Mislabeled Coffee Cake Due to Undeclared Walnuts

The James Skinner LLC is conducting a voluntary recall of a single lot of Publix Maple Walnut Coffee Cake as the wrong ingredient label was applied to the packaging on certain units. Product was packaged in cases with Maple Walnut Coffee Cake labels but then inadvertently individually labeled as Publix Raspberry Coffee Cake.  This resulted in undeclared walnuts.

Observable through the clear lid, the product has visible walnuts on top of the cake and brown maple topping, whereas Raspberry Coffee Cake has no walnuts on top and red topping. The issue was discovered by a retail store employee who observed the visible walnuts on top of the product and noticed that the product had a Raspberry Coffee Cake label instead of a Maple Walnut Coffee Cake label.

Unfortunately, a quality check did not catch the issue when it was produced.  Clearly, an Allergen Preventive Control for ensuring the proper label is applied is needed in this baking operation, where one could guess that there are a number of different products labeled.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/james-skinner-llc-issues-voluntary-recall-publix-maple-walnut-coffee-cake-due-incorrect-labeling

The James Skinner LLC Issues Voluntary Recall of Publix Maple Walnut Coffee Cake Due to Incorrect Labeling
Summary
Company Announcement Date:  December 10, 2025
FDA Publish Date:  December 16, 2025
Product Type:  Food & Beverages  Allergens
Reason for Announcement:  Label does not declare walnuts in the ingredient list.
Company Name:  The James Skinner LLC
Brand Name:  Publix
Product Description:  Publix Raspberry Coffee Cake

Frozen Dessert Products Recalled for Foreign Materials in the Cluster Component

Danone U.S. is voluntarily recalling its So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints with multiple best-by expiration dates before 08 Aug 2027 at retail stores nationwide due to the potential presence of foreign materials, such as small stones and other hard objects, within the cashew inclusions.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-salted-caramel-cluster-frozen-dessert-pints-voluntarily-recalled-danone-us
So Delicious Dairy Free® Salted Caramel Cluster Frozen Dessert Pints Voluntarily Recalled by Danone U.S. Due to Potential Presence of Foreign Material
Summary
Company Announcement Date:  December 15, 2025
FDA Publish Date:  December 15, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Potential presence of foreign materials such as stones and other hard objects.
Company Name:  Danone U.S.
Brand Name:  So Delicious
Product Description:  Non-dairy frozen dessert

Virginia Firm Recalls Cakes Where Undeclared Soy Is Used to Solve Sticking Issue

Ukrop’s Homestyle Foods, LLC, Richmond, VA announced today that it is recalling four of its Decorated Pound Cakes due to an undeclared soy allergen.  A cake releasing agent containing soy was used to prevent sticking for the cakes listed below only.

So this is probably a case where the anti-sticking / pan release agent contained soy lecithin.  The scenario probably goes like this....the facility has a sticking issue on one day of production, and someone sprays on the pan release agent to solve the issue unaware it just created a recallable situation with an undeclared allergen.

This is where employee training on allergens is so important. Also, restrictions on changing process without a thorough review.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ukrops-homestyle-foods-announces-recall-due-undeclared-allergen
Ukrop’s Homestyle Foods Announces Recall Due to Undeclared Allergen
Summary
Company Announcement Date:  December 11, 2025
FDA Publish Date:  December 15, 2025
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared soy
Company Name:  Ukrop;s Homestyle Foods, LLC
Brand Name: Ukrop’s
Product Description:  Decorated pound cakes

FDA Issues Warning Letter to RTE Seafood Processor After Inspection and Poor Environmental Monitoring Results

FDA issued a Warning Letter to Harbor Marine Product Inc., Vernon, CA, a  processor of raw, ready-to-eat (RTE) fish.  FDA analysis found Listeria species (non-pathogenic strains) in the facility as well as identified many product handling issues that could lead to contamination of the RTE product.  

One takeaway from this is that Listeria is an food facility environmental hazard in sushi-grade RTE seafood.  This is one reason why the American College of Obstetricians and Gynecologists recommends that pregnant woman avoid all raw or undercooked fish.

FDA laboratory analysis found that (b)(4) of the (b)(4) environmental swabs were positive for non-pathogenic Listeria spp., including Listeria innocua, Listeria welshimeri, and Listeria grayi. Of the (b)(4) positive swabs, (b)(4)% ((b)(4) swabs) were collected from food contact surfaces in areas where raw, RTE salmon and tuna are processed. The positive food contact surfaces included:

• cutting board surface on fillet tables where raw, RTE salmon was touching;

• surfaces of tools, including pliers and knives, used to directly cut and manipulate raw, RTE salmon;

• table dividers, edges, and corners where raw, RTE tuna and salmon contacts;

• blade and handle of knife in ice bed used to cut raw, RTE tuna;

• water drain hole at the end of table where raw, RTE salmon is handled;

• cutting board surface of corner fillet table (where condensate was observed dripping from the air conditioning unit) where raw, RTE tuna and salmon contacts.

This demonstrates the facility's sanitation procedures have been inadequate to effectively control microbiological contamination in the facility. 

There were "numerous serious insanitary conditions and practices were observed in [the] facility during [the] FDA inspection."  Many of these issues would facilitate contamination of the RTE product with Listeria.

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/harbor-marine-product-inc-710589-11282025
Harbor Marine Product Inc.
MARCS-CMS 710589 — November 28, 2025
Warning Letters

FDA Issues Warning Letters to Major Retailers for Failure to Remove Recalled Baby Formula

FDA issued Warning Letters to major retailers for failure to properly respond to the recall of ByHeart baby formula that was linked to botulism cases in infants.  Kroger, Walmart, Albertsons and Target were issued Warning Letter stating the the retailers did not properly conduct the needed corrective actions to remove product from the store shelves in a timely manner.  This is a reminder to entire industry for the need to properly respond to recall notices.

In a notice to the industry, FDA stated that inspectors "had checked retail stores across the U.S. over 4,000 times to ensure recalled product was not being made available to consumers. Through this effort, we found that recalled infant formula continued to be found on store shelves—for over three weeks in one case, in over 175 locations across 36 states."

Here are the highlights for the Warning Letter to Kroger.

• The Kroger Company (Kroger) was notified on November 8, 2025, of this voluntary recall. On November 11, 2025, ByHeart expanded the recall to all ByHeart Whole Nutrition Infant Formula, including all unexpired lots of formula cans and single-serve “anywhere pack” sticks. As a consignee of the recalled products, Kroger was notified in writing on November 11, 2025, that the scope of the voluntary recall had expanded to include all ByHeart infant formula products. Despite these recall notifications, subsequent visits by regulators confirmed that recalled ByHeart Whole Nutrition Infant Formula remained available for purchase on shelves at (b)(4) Kroger stores, including Kroger’s, King Sooper’s, and Smith’s, across 10 states well after the recall was initiated and subsequently expanded.
• However, based on FDA’s review of information from state and local partners, the Agency determined that recalled ByHeart Whole Nutrition Infant Formula remained on shelves at (b)(4) Kroger store locations across 10 states from November 12, 2025, to November 19, 2025. This represents a period of (b)(4) days after Kroger was first notified of the initial recall and (b)(4) days after Kroger was notified of the recall expansion
• On November 18, 2025, FDA held a call with you to discuss the ineffectiveness of the recall within your Walmart stores. During this discussion, FDA requested information regarding actions you were prepared to implement to ensure recalled product was no longer available for purchase at Walmart stores nationwide. Despite follow-up emails from the FDA on November 20, 21, and 24, 2025, and December 1, 3, and 8, 2025, you have not provided FDA with any information demonstrating that corrective actions to effectuate this recall have been implemented throughout your organization to prevent adulterated food from being received in interstate commerce and subsequently offered for sale.

Walmart, Albertsons and Target were issued similar letters with similar findings in failure to properly respond.

US Food and Drug Administration
https://content.govdelivery.com/accounts/USFDA/bulletins/4000713
FDA Takes Action to Improve Recall Effectiveness Following Infant Botulism Outbreak Investigation Linked to ByHeart Infant Formula
U.S. Food and Drug Administration sent this bulletin at 12/15/2025 04:14 PM EST

Another Salmonella Outbreak Linked to Eggs in California

The California Dept of Health reported that 63 people have become ill with Salmonella Enteritidis infection from eggs from Vega Farms, Inc. in Dixon, CA.

According to one report, "After identifying the supplier of the suspect eggs, CDPH and CDFA conducted an inspection at Vega Farms, Inc. and collected egg and environmental samples for testing. Multiple samples tested positive for Salmonella. Whole genome sequencing analysis revealed that the Salmonella in at least one sample matched the strain found in sick individuals. Vega Farms eggs were sold to restaurants, grocery stores, co-ops, and in farmers markets in Northern California."

While no one likes to say it, Salmonella control is more difficult for operations with open range chickens.  Advise should be for cooking those eggs thoroughly.


https://www.independent.com/2025/12/12/cdph-warns-consumers-not-to-eat-recalled-vega-farms-inc-in-shell-eggs/

CDPH Warns Consumers Not to Eat Recalled Vega Farms, Inc. In-shell Eggs

By California Department of Public Health

Fri Dec 12, 2025 | 12:13pm

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FDA Provides Update on Infant Botulism Outbreak (12/10/25)

In the most recent update, CDC broadened the timeframe associated with the ByHeart product.  "CDC broadened the case definition to include any infant with botulism who was exposed to ByHeart formula at any time since the product’s release in March 2022. As of December 10, 2025, a total of 51 infants with suspected or confirmed infant botulism and confirmed exposure to ByHeart Whole Nutrition infant formula (various lots) have been reported from 19 states."

"Previously, case counts included illnesses from August 1, 2025, onward. With the expanded definition, CDC and state partners identified 10 additional prior cases that occurred from December 2023 through July 2025. At this time, no cases have been identified between March 2022 and December 2023. All 10 prior cases are confirmed infant botulism cases with documented exposure to ByHeart formula."

"FDA’s investigation is ongoing to determine the point of contamination."

Case Counts
Total Illnesses: 51 (12 New)
Hospitalizations: 51 (12 New)
Deaths: 0
Last Illness Onset: December 1, 2025
States with Cases: AZ, CA, ID, IL, KY, MA, ME, MI, MN, NC, NJ, OH, OR, PA, RI, TX, VA, WA, WI
Product Distribution: Online and nationwide (including Guam and Puerto Rico), and internationally

The previous update was 12/3/25.

https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-infant-botulism-infant-formula-november-2025
Outbreak Investigation of Infant Botulism: Infant Formula (November 2025)
Do not use recalled ByHeart Whole Nutrition Infant Formula. FDA’s investigation is ongoing.

Food Companies Push Back on Texas Law Requiring Warning Label for Certain Ingredients

Food companies are suing the State of Texas after the state's new law requiring warning labels for over 40 different ingredients.  "Section 9 of the law requires food manufacturers to include warning labels on products that include 44 listed ingredients, including artificial additives, dyes and chemicals, informing customers that governments in Australia, Canada, the European Union, or the United Kingdom have labeled the ingredients as “not recommended for human consumption.”"  Note, this is not based upon what the US has determined, but what other countries have determined.

From the Texas Rule

Sec. 431.0815.  FOOD CONTAINING ARTIFICIAL COLOR, ADDITIVES, OR CERTAIN BANNED CHEMICALS. (a) A food manufacturer shall ensure each food product the manufacturer offers for sale in this state includes a warning label disclosing the use of any of the following ingredients, if the United States Food and Drug Administration requires the ingredient to be named on a food label and the ingredient is used in a product intended for human consumption:

The warning label must:  (1)  include the following statement if the food contains an ingredient listed in Subsection (a), printed in a font size not smaller than the smallest font used to disclose other consumer information required by the United States Food and Drug Administration:

“WARNING: This product contains an ingredient that is not recommended for human consumption by the  appropriate authority in Australia, Canada, the European Union, or the United Kingdom.";

Many of these ingredients have been long used in the US and are in many of the foods we eat....well, foods I eat....you know, those highly processed foods like potato chips and snack cakes.

Here are some from the list which I knew to be readily used.

(Entire list - https://legiscan.com/TX/text/SB25/id/3247967  about half way down the webpage)

• Bleached flour is treated white flour treated creating a softer texture that absorbs more liquid, making it great for delicate cakes, cookies, and pie crusts
• BHA and BHT - synthetic antioxidants used as preservatives in foods (cereals, chips, meats, etc) to prevent fats and oils from going rancid
• Diacetyl occurs naturally and it gives butter its characteristic taste. Because of this, manufacturers of artificial butter flavoring, margarines or similar oil-based products typically add diacetyl to give that characteristic aroma/flavor.
• Potassium aluminum sulfate is a firming agent for pickles, leavening in baking, pH control
• Sodium aluminum sulfate is used in baking powder as a slow-acting leavening agent
• Sodium Lauryl Sulfate is an emulsifier/thickener in some dried eggs, marshmallows, and beverage bases
• Stearyl tartrate is an emulsifier and dough strengthener to improve dough texture
• Stearyl tartrate acts as a dough strengthener, emulsifier, and stabilizer in foods, improving consistency

To heck with the sugar in that pack of Ho-Hos, it is the dough conditioner you have to worry about.

Reuters
https://www.reuters.com/legal/government/food-industry-groups-sue-texas-over-ingredient-warning-labels-2025-12-08/
Food industry groups sue Texas over ingredient warning labels
By Dietrich Knauth

December 8, 20251:54 PM ESTUpdated December 8, 2025

NY Distributor Recalls Bangladeshi Indian Snack Mix After State Lab Detects Undeclared Peanuts

South Asian Food Inc. of Maspeth, Queens, NY is recalling its 12.34oz (350gm) packages of Bengal King Jhal Chanachur food treats because they may contain undeclared peanuts.   The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed that the peanut-containing product was distributed in packages that did not reveal the presence of peanuts.

The recalled Bengal King Jhal Chanachur were distributed nationwide in retail stores and through mail orders. 

"Chanachur or Bombay mix is a Bangladeshi Indian snack mix (namkeen) which consists of a variable mixture of spicy dried ingredients, such as fried lentils, peanuts, chickpea flour ghatia (sev), corn, vegetable oil, chickpeas, flaked rice, fried onion and curry leaves. This is all flavored with salt and a blend of spices that may include coriander and mustard seed." (Ref)


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/south-asian-food-inc-issues-allergy-alert-undeclared-peanuts-bengal-king-jhal-chanachur
South Asian Food Inc. Issues Allergy Alert on Undeclared Peanuts in "Bengal King Jhal Chanachur "
Summary
Company Announcement Date:  December 12, 2025
FDA Publish Date:  December 12, 2025
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared peanut allergen
Company Name:  South Asian Food Inc
Brand Name:  Bengal King
Product Description:  Jhal Chanachur food treats

Ohio Foodservice Establishment Recalls Mispackaged Sliders Undeclared Allergens Associated with Jalapeno Cheese

White Castle Frozen Food Division, Columbus, OH has initiated a recall of 1,021 cases of its retail frozen 4-count cartons of Original Sliders due to undeclared milk and soy. The carton may contain Jalapeño Cheese Sliders. Jalapeño Cheese Sliders contain milk and soy, allergens that are not on the Original Slider carton label.

During the packaging process, Jalapeño Cheese Sliders were put in the wrong package, and milk and soy are not listed as ingredients or allergens on the packaging. The issue was discovered when a customer notified White Castle that they suffered a non-life-threatening allergic reaction after consuming one of the Jalapeño Cheese Sliders that was incorrectly packaged in the 4-count Original Sliders carton. No other reports of injury or illness have been received to date.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/white-castle-frozen-food-division-recalls-frozen-4-count-cartons-original-sliders-due-undeclared
White Castle Frozen Food Division Recalls Frozen 4-Count Cartons of Original Sliders Due to Undeclared Milk and Soy
Summary
Company Announcement Date:  December 12, 2025
FDA Publish Date:  December 12, 2025
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared milk and soy allergens
Company Name:  White Castle Food Products LLC
Brand Name:  White Castle
Product Description:  Original Sliders, frozen, 4 count carton