Check the Batch
Class ITerminated in FDA datasetRecall initiated Sep 20, 2013

Market Pantry Tuna 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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 11, 2014.

Check your package

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

ProductMarket Pantry Tuna Salad, UPC 0 85239 24108 0, 12 oz., Product Code 24108. Weis Tuna Salad, UPC 0 41497 05345 2, 6 x 8 oz, Product Code 05345
Package size12 oz
UPC041497053452, 085239241080

FDA code information

Code Date for 24108 = 9/24/2013 - 10/10/2013; 05345 = 09/24/2013 - 10/14/2013

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

Full FDA record and distribution details

Original product description

Market Pantry Tuna Salad, UPC 0 85239 24108 0, 12 oz., Product Code 24108. Weis Tuna Salad, UPC 0 41497 05345 2, 6 x 8 oz, Product Code 05345

Extracted codes and context

TypeCode / valueContext
UPC041497053452na Salad, UPC 0 85239 24108 0, 12 oz., Product Code 24108. Weis Tuna Salad, UPC 0 41497 05345 2, 6 x 8 oz, Product Code 05345
UPC085239241080Market Pantry Tuna Salad, UPC 0 85239 24108 0, 12 oz., Product Code 24108. Weis Tuna Salad, UPC 0 41497 05345 2, 6 x 8 oz, Product Code 05345

Original FDA recall reason

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.

Recall details

Recall number
F-0458-2014
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-0458-2014

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

Follow official FDA and manufacturer guidance.