Recalled by Almark Foods, LLC · Gainesville, GA, United States
Class I — High risk. Reasonable probability of serious harm or death.
The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
Bulk Pail Product - Almark Foods HARD COOKED EGGS Peeled Eggs INGREDIENTS: EGGS, WATER, CITRIC ACID sold under the following brand names: ALMARK EGGS 20 LB pail, Manufactured By: Almark Foods Gainesville, GA 30504 UPC 0 44984 30020 6; Egggs NET WT WHEN PACKED 23 LBS Distributed by: Carolina Egg Development Corporation 5645 Deans Street, Bailey, NC 27807 UPC o 29653 00599 6; Nic's Peeled Pearls 20 lb. Salad Grade Hard Boiled Eggs NET WT. WHEN PACKED 20 LBS UPC 1 00 39401 17395 9 & 23LBS UPC 1 00 39401 00011 8 Manufactured By: Almark Foods Gainesville, GA 30504; RAINBOW FARMS 20 LB UPC 0 44984 60020 7, 23 LB UPC 0 44984 60023 8, 25 LB UPC 0 44984 60025 2 Manufactured By: Almark Foods Gainesville, GA 30504 & SUTHERLAND'S FOOD SERVICE INC. NET WT. 20 LBS.
Quantity: 6,854 various size pails
Food: Eggs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Almark: ITEM #30020 BEST IF USED BY 1/29/2020, 2/10/2020, 2/24/2019 & 2/14/2020. Egggs: ITEM #64023-05 BEST IF USED BY 1/27/2020 Nics: ITEM #17394 BEST IF USED BY 1/20/2020, 2/3/2020, 2/4/2020 & 2/24/2020 Nics: ITEM #17295 BEST IF USED BY 12/24/2019, 12/25/2019, 12/31/2019, 1/6/2020, 1/7/2020, 1/8/2020, 1/13/2020, 1/14/2020, 1/28/2020, 1/28/2020, 1/29/2020, 2/4/2020, 2/5/2020 Rainbow: ITEM #60020 BEST IF USED BY 1/13/2020, 1/20/2020, 1/21/2020, 1/22/2020, 1/27/2020, 1/28/2020, 1/29/2020, 2/3/2020, 2/10/2020, 2/11/2020, 2/14/2020, 2/17/2020, 2/18/2020, 2/24/2020 Rainbow: ITEM #60023 BEST IF USED BY 1/13/2020, 1/15/2019, 1/20/2020, 1/22/2019, 1/27/2020, 1/29/2020, 2/3/2020, 2/10/2020, 2/13/2020, 2/17/2020, 2/19/2020, 2/24/2020, 2/26/2020 Rainbow: ITEM #60025 BEST IF USED BY 1/13/2020, 1/28/2020, 2/13/2020, 2/17/2020 Sutherland: ITEM #60020-3 BEST IF USED BY 1/15/2020
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FDA's distribution note: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI & WY.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
FDA files each product of one recall action separately; these share the same FDA event.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
Reason The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
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Reason The firm was notified by their customer that the product is missing the back panel containing the ingredient, nutrition and allergen statements. Product contains eggs and milk.
Reason FDA notified the firm of positive test results for Listeria monocytogenes found in the firm.