Eagle Produce LLC Scottsdale, AZ is initiating a recall of 224 cases of whole cantaloupe because they have the potential to be contaminated with Salmonella. The recall is the result of routine sample testing conducted by the State of Michigan which revealed the presence of Salmonella in cantaloupe sold at retail. There have been no reported illnesses. The products were distributed between August 13th - 17th in Michigan, Missouri, Ohio, Texas and Virginia and sold in various retail supermarkets.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eagle-produce-llc-recalls-whole-cantaloupe-because-possible-health-risk-0
Eagle Produce LLC Recalls Whole Cantaloupe Because of Possible Health Risk
Summary
Company Announcement Date: September 06, 2024
FDA Publish Date: September 06, 2024
Product Type: Food & Beverages Fruit/Fruit Product
Reason for Announcement: Potential to be contaminated with Salmonella
Company Name: Eagle Produce LLC
Brand Name: Kandy
Product Description: Whole Cantaloupe
Monday, September 9, 2024
CA Firm Recalls Shiso Katsuo Ninniku
Niitakaya USA Inc. of Montebello, CA, is recalling All Best By dates of its 5.2 ounce (147 gram) packages of #3700 Shiso Katsuo Ninniku /#3701 Miso Katsuo Ninniku because they may contain undeclared Allergen of Fish (Bonito). The recall was initiated after it was discovered that product containing Fish (Bonito) was distributed in packaging that did not reveal the presence of “Containing allergen: Fish (Bonito)”.
Shiso Katsuo Ninniku is a pickled product.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/niitakaya-usa-inc-issues-allergy-alert-undeclared-allergen-fish-bonito-3700-shiso-katsuo-ninniku3701
Niitakaya USA Inc. Issues Allergy Alert on Undeclared Allergen of Fish (Bonito) in #3700 Shiso Katsuo Ninniku/#3701 Miso Katsuo Ninniku
Summary
Company Announcement Date: September 04, 2024
FDA Publish Date: September 05, 2024
Product Type: Food & Beverages
Reason for Announcement: Undeclared Fish (Bonito)
Company Name: Niitakaya USA Inc.
Brand Name: Niitakaya
Product Description: Shiso Katsuo Ninniku & Miso Katsuo Ninniku
Shiso Katsuo Ninniku is a pickled product.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/niitakaya-usa-inc-issues-allergy-alert-undeclared-allergen-fish-bonito-3700-shiso-katsuo-ninniku3701
Niitakaya USA Inc. Issues Allergy Alert on Undeclared Allergen of Fish (Bonito) in #3700 Shiso Katsuo Ninniku/#3701 Miso Katsuo Ninniku
Summary
Company Announcement Date: September 04, 2024
FDA Publish Date: September 05, 2024
Product Type: Food & Beverages
Reason for Announcement: Undeclared Fish (Bonito)
Company Name: Niitakaya USA Inc.
Brand Name: Niitakaya
Product Description: Shiso Katsuo Ninniku & Miso Katsuo Ninniku
Salmonella Outbreak Linked to Wisconsin Egg Producer, Firm Recalls Eggs
A Salmonella outbreak has been linked to Milo's Poultry Farms. CDC and FDA are investigating this outbreak of Salmonella Enteritidis infections with 65 reported cases with 24 hospitalizations covering 9 states. FDA conducted an inspection at Milo’s Poultry Farms and collected samples. FDA’s analysis showed the outbreak strain of Salmonella was found in the packing facility and the hen egg laying house.
Milo’s Poultry Farms, LLC. of Bonduel, WI is recalling all “Milo’s Poultry Farms” and “Tony’s Fresh Market” branded eggs because these eggs have the potential to be contaminated with Salmonella. Milo’s Poultry Farms, LLC. has ceased production and distribution at this time and will undergo appropriate testing and sanitization of farms and processing equipment.
CDC Food Safety Alert
https://www.cdc.gov/salmonella/eggs-09-24/index.html
Salmonella Outbreak Linked to Eggs
Fast Facts
Illnesses: 65
Hospitalizations: 24
Deaths: 0
States: 9
Investigation status: Active
Milo’s Poultry Farms, LLC. of Bonduel, WI is recalling all “Milo’s Poultry Farms” and “Tony’s Fresh Market” branded eggs because these eggs have the potential to be contaminated with Salmonella. Milo’s Poultry Farms, LLC. has ceased production and distribution at this time and will undergo appropriate testing and sanitization of farms and processing equipment.
CDC Food Safety Alert
https://www.cdc.gov/salmonella/eggs-09-24/index.html
Salmonella Outbreak Linked to Eggs
Fast Facts
Illnesses: 65
Hospitalizations: 24
Deaths: 0
States: 9
Investigation status: Active
Thursday, September 5, 2024
Alabama Establishment Recalls Jerky Produced Without FSIS Inspection
Hickory Hollow Jerky, a Eufaula, Ala., establishment, is recalling approximately 6,229 pounds of ready-to-eat jerky products that were produced without the benefit of federal inspection. The beef jerky and bacon jerky products were produced on various dates between Jan. 19, 2024-Aug. 21, 2024. The products were produced without the benefit of inspection by two different owners of the establishment. Ownership changed hands on June 11, 2024. The problem was discovered during routine FSIS surveillance activities when it was determined that the establishment continued to produce these jerky products and label them with the USDA mark of inspection after requesting to voluntarily stop FSIS-inspection activities.
https://www.fsis.usda.gov/recalls-alerts/hickory-hollow-jerky-recalls-ready-eat-jerky-products-produced-without-benefit
Hickory Hollow Jerky Recalls Ready-To-Eat Jerky Products Produced Without Benefit of Inspection
WASHINGTON, Aug. 30, 2024 – Hickory Hollow Jerky, a Eufaula, Ala., establishment, is recalling approximately 6,229 pounds of ready-to-eat jerky products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
https://www.fsis.usda.gov/recalls-alerts/hickory-hollow-jerky-recalls-ready-eat-jerky-products-produced-without-benefit
Hickory Hollow Jerky Recalls Ready-To-Eat Jerky Products Produced Without Benefit of Inspection
WASHINGTON, Aug. 30, 2024 – Hickory Hollow Jerky, a Eufaula, Ala., establishment, is recalling approximately 6,229 pounds of ready-to-eat jerky products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
FDA Issues Warning Letter to CA Firm Selling Goat Milk as Infant Formula
FDA issued a Warning Letter to a CA company selling goat milk for toddlers. According to the Warning Letter the product, Sammy’s Milk, is considered an infant formula under section 201(z) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321(z)] because it is a food which purports to be or is represented for special dietary use solely as a food for infants by reason of its simulation of human milk or its suitability as a complete or partial substitute for human milk. However, the do not meet the standards for infant formula.
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/graceleigh-inc-dba-sammys-milk-682538-08142024
Graceleigh, Inc. dba Sammy’s Milk
MARCS-CMS 682538 — August 14, 2024
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/graceleigh-inc-dba-sammys-milk-682538-08142024
Graceleigh, Inc. dba Sammy’s Milk
MARCS-CMS 682538 — August 14, 2024
Warning Letter Issued to Hawaii Water Processor
FDA inspected a bottled water manufacturing facility located in Hilo, HI and issued a Warning Letter to that firm. For one, the treatment of product water was not done in a manner that was effective in accomplishing the intended purpose. In fact, the firm started receiving consumer complaints regarding foreign material including but not limited to apparent “mold”, “white blob”, and “floaters” in 1-liter bottles of its Waiakea Hawaiian Volcanic Water. A third-party laboratory found "heterotrophic plate count (HPC) at >5700 CFU/mL, Pseudomonas aruginosa at >2400 MPN/100mL, and mold at 15 CFU/mL." Also, "the process controls did not include, as appropriate to the nature of the applicable control and its role in the facility's food safety system, parameters associated with the control of a hazard, as required by 21 CFR 117.135(c)(1)(i)"
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/waiakea-bottling-inc-681285-08132024
Waiakea Bottling Inc.
MARCS-CMS 681285 — August 13, 2024
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/waiakea-bottling-inc-681285-08132024
Waiakea Bottling Inc.
MARCS-CMS 681285 — August 13, 2024
Illinois Food Company Recalls Cinnamon Powder After State Lab Detects Lead
Asli Fine Foods of Woodridge, IL is recalling Asli Cinnamon Powder 7 oz, because it has the potential to be contaminated with Lead. Product was distributed MN, IN, IL, MO & OH it reached consumers through retail stores. The recall was the result of a routine sampling program by the Missouri Department of Health and Senior Services which revealed that the finished products contained Lead. The company has ceased the production and distribution of the product as FDA and the company continue their investigation as to what caused the problem.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/asli-fine-foods-recalls-asli-cinnamon-powder-7-oz-because-possible-health-risk
Asli Fine Foods . Recalls Asli Cinnamon Powder 7 oz Because of Possible Health Risk
Summary
Company Announcement Date: August 29, 2024
FDA Publish Date: August 30, 2024
Product Type: Food & Beverages
Reason for Announcement: Contains Lead
Company Name: Asli Fine Foods
Brand Name: Asli Fine Foods
Product Description: Cinnamon powder
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/asli-fine-foods-recalls-asli-cinnamon-powder-7-oz-because-possible-health-risk
Asli Fine Foods . Recalls Asli Cinnamon Powder 7 oz Because of Possible Health Risk
Summary
Company Announcement Date: August 29, 2024
FDA Publish Date: August 30, 2024
Product Type: Food & Beverages
Reason for Announcement: Contains Lead
Company Name: Asli Fine Foods
Brand Name: Asli Fine Foods
Product Description: Cinnamon powder
Friday, August 30, 2024
CDC Provides Update on Listeria Outbreak Linked to Deli Meat
CDC provided an update of the Listeria outbreak linked to Boar's Head deli meat. Since the last update on August 8, 14 more illnesses and six more deaths have been reported. As of August 27, a total of 57 people infected with the outbreak strain of Listeria have been reported from 18 states. S Of 57 people with information available, all 57 have been hospitalized. There have been 9 deaths.
CDC Food safety alert
https://www.cdc.gov/listeria/outbreaks/delimeats-7-24.html
Listeria Outbreak Linked to Meats Sliced at Delis
August 28, 2024
Investigation start date: July 19, 2024
Investigation status: Open
Recall issued: Yes
Latest update: More illnesses and deaths have been reported in this outbreak. Listeria is a hardy germ that can remain on surfaces, like meat slicers, and foods, even at refrigerated temperatures. It can also take up to 10 weeks for some people to have symptoms of listeriosis. Do not eat recalled deli meats. Some of the products have sell by dates into October 2024.
Fast Facts
Cases: 57 (14 new)
Hospitalizations: 57 (14 new)
Deaths: 9 (6 new)
States: 18 (5 new)
CDC Food safety alert
https://www.cdc.gov/listeria/outbreaks/delimeats-7-24.html
Listeria Outbreak Linked to Meats Sliced at Delis
August 28, 2024
Investigation start date: July 19, 2024
Investigation status: Open
Recall issued: Yes
Latest update: More illnesses and deaths have been reported in this outbreak. Listeria is a hardy germ that can remain on surfaces, like meat slicers, and foods, even at refrigerated temperatures. It can also take up to 10 weeks for some people to have symptoms of listeriosis. Do not eat recalled deli meats. Some of the products have sell by dates into October 2024.
Fast Facts
Cases: 57 (14 new)
Hospitalizations: 57 (14 new)
Deaths: 9 (6 new)
States: 18 (5 new)
FDA Issues Warning Letter to Small Sprout Operation
FDA issued a Warning Letter to a small sprout farm operation located in Pennsylvania. The facility operates as a qualified facility under modified requirements. However, FDA does tell the facility that the application of modified requirements can be removed by the FDA is warranted, then it would be subject to all relevant requirements in the Produce Safety Rule
Issues noted in the Warning Letter:
WARNING LETTER
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/pl-bean-sprout-farm-680777-07312024
- FDA investigators observed gray sludge falling from the railing where the automatic sprinkler system is mounted and accumulating in sprouts growing below. The company told our investigator that this gray sludge was food-grade oil. However, the company was not able to provide FDA investigators the container or labeling of the apparent oil. Further, the substance appeared dirty. Further, during the inspection closeout meeting, the company stated that the sprouts that may have become contaminated would be discarded, however, the company had introduced into commerce the sprouts observed on that date. In addition, the company did not address how to prevent the contamination of in-process sprouts in the future.
- FDA observed apparent rodent excreta pellets underneath a table in the packaging room, where packaging material used for ready to eat (RTE) mung bean sprouts was being stored. This finding demonstrates that rodents have access to food contact surfaces and may have directly or indirectly contaminated the sprouts with feces. The third-party pest control company documented rodent activity on November 28, 2023, December 26, 2023, and January 23, 2024, and recommended actions to prevent recurrence, however, the company did not implement any of these recommended actions.
- Facility issues included a) The ceiling in the sprout processing area has peeling and chipped paint, and apparent cobwebs and insect frass directly above the open sprout harvesting machine. b) The floor directly under the sprout harvesting machine in the sprout processing area was wet, pitted, and cracked. This may cause the floor to be a harborage site for pathogens.
- On January 31, 2024, and February 1, 2024, FDA investigators observed a pressurized hose used to rinse food contact surface equipment and in-process sprouts frayed and stored on the floor in the sprout production room. This may have resulted in the contamination of your sprouts with any substances, including any pathogens, from the floor. Furthermore, the hose described above was used without being cleaned or sanitized. An employee with gloved hands touched the circuit breaker, cleaned a seed bed, handled the hose, and then returned to handling sprouts without either changing their gloves or removing the gloves and handling the sprouts with clean hands. This may have resulted in the gloves contaminating the sprouts with any substances contacting the gloves prior to hose handling.
- During the inspection, we observed that an exit door is in poor repair and unable to fully close to exclude pests from entering the facility. Additionally, there were harborage conditions around the perimeter of the facility that potentially attract pests, including sprouts around the external cement block of the unplugged trash receptacle and empty plastic containers behind the building.
WARNING LETTER
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/pl-bean-sprout-farm-680777-07312024
P&L Bean Sprout Farm
MARCS-CMS 680777 — July 31, 2024
MARCS-CMS 680777 — July 31, 2024
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