FDA recall record

Reser's Fine Foods Freshness Guaranteed Macaroni Salad Amish, item # 579284 recall — FDA F-0454-2021

Undeclared Wheat and/or Egg. The bottom label of Macaroni Salad Amish was mis-labeled as Red Potatoes salad or Baked Beans. The label of the Red Potatoes…

Class IIclassification
F-0454-2021official record ID
Apr 28, 2021report date

Recall record at a glance

Official recordF-0454-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmReser's Fine Foods, Inc.
Report dateApr 28, 2021
Recall initiation dateApr 14, 2021
QuantityTotal 16,614/32 oz. Packages or 2769 Cases (6/32 oz. packages per case)
LocationBeaverton, OR, United States

Official product description

Freshness Guaranteed Macaroni Salad Amish, item # 579284, refrigerated, packaged in a clear cup with clear snap on lid, net wt. 32 oz. UPC 0 78742 13235 8. Each master case containing 6/32 oz. packages. Distributed by: Walmart Inc, Bentonville, AR. The CORRECT label is read in parts: "***FRESHNESS GUARANTEED MACACONI SALAD Amish *** INGREDIENTS: COOKED ENRICHED MACARONI (SEMOLINA, EGG WHITES ***), HARD COOKED EGG***CONTAINS EGGS AND WHEAT***". The INCORRECT bottom label is read parts: "***INGREDIENTS: BEANS***RED PEPPER POWDER***". The INCORRECT bottom label is read parts: "***INGREDIENTS: RED POTATOES, MAYONNAISE (***EGG YOLK***)*** CONTAINS EGGS ***".

Why the product was recalled

Undeclared Wheat and/or Egg. The bottom label of Macaroni Salad Amish was mis-labeled as Red Potatoes salad or Baked Beans. The label of the Red Potatoes salad declares EGG only but does not declare WHEAT. The label of the Baked Beans does not declare EGG and WHEAT.

Distribution information

Distributed in AR, IL, IN, MN ,MO, OK WI, and WY.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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

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