FDA recall record

Almark Foods WATER, CITRIC ACID sold under the following brand names recall — FDA F-0603-2020

The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient…

Class Iclassification
F-0603-2020official record ID
Feb 12, 2020report date

Recall record at a glance

Official recordF-0603-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmAlmark Foods, LLC
Report dateFeb 12, 2020
Recall initiation dateDec 19, 2019
Quantity6,854 various size pails
LocationGainesville, GA, United States

Official product description

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.

Why the product was recalled

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.

Distribution information

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.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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