Class ITerminated in FDA datasetSep 20, 2013

Weis Potato with Egg Salad

Recalling firm: Garden-Fresh Foods, Inc.

Why it was recalled

Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products sold under various brands and codes because they may be contaminated with Listeria monocytogenes.

Check your package

Compare the exact product and package details with the label you have.

ProductWeis Potato with Egg Salad, UPC 0 41497 05841 9, 16 oz, Product Code 05841. Weis Potato Salad with Egg, UPC 0 41497 05902 7, 3 lb., Product Code 05902. Weis Potato Salad with Egg, UPC 0 11596 51101 6, 2/5 lb., Product Code 1101
UPC011596511016, 041497058419, 041497059027

FDA code information

Code Date 05841 = 09/24/2013 - 10/10/2013. 05902 = 10/2/2013 - 10/10/2013 1101 = 10/2/2013 - 10/10/2013

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Weis Potato with Egg Salad, UPC 0 41497 05841 9, 16 oz, Product Code 05841. Weis Potato Salad with Egg, UPC 0 41497 05902 7, 3 lb., Product Code 05902. Weis Potato Salad with Egg, UPC 0 11596 51101 6, 2/5 lb., Product Code 1101

Extracted codes and context

TypeCode / valueContext
UPC011596511016UPC 0 41497 05902 7, 3 lb., Product Code 05902. Weis Potato Salad with Egg, UPC 0 11596 51101 6, 2/5 lb., Product Code 1101
UPC041497058419Weis Potato with Egg Salad, UPC 0 41497 05841 9, 16 oz, Product Code 05841. Weis Potato Salad with Egg, UPC 0 41497 05902 7, 3 lb., Product Code 05902. Weis Potato Sal
UPC041497059027UPC 0 41497 05841 9, 16 oz, Product Code 05841. Weis Potato Salad with Egg, UPC 0 41497 05902 7, 3 lb., Product Code 05902. Weis Potato Salad with Egg, UPC 0 11596 51101 6, 2/5 lb., Product Code 1101

Recall details

Recall number
F-0426-2014
Event ID
66623
FDA status
Terminated
Initiated
Sep 20, 2013
Reported
Dec 18, 2013
Classified
Dec 10, 2013
Terminated
Feb 11, 2014
Quantity
94,346 total cases, for all varieties
Location
Milwaukee, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

nationwide

FDA source record · F-0426-2014

Data updated September 16, 2026. View official FDA data ↗

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