Check the Batch
Class ITerminated in FDA datasetRecall initiated Oct 22, 2013

Walmart Deli Potato Salad, Formula PO.121, packaged in 12/16-oz (

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

The recalled products are potentially contaminated with Listeria monocytogenes.

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: Jan 24, 2017.

Check your package

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

ProductWalmart Deli Potato Salad, Formula PO.121, packaged in 12/16-oz (UPC 681131916783), 6/32-oz (UPC 681131916844) and 6/4-lb (UPC 681131916905) carton cases. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR.
UPC681131916783, 681131916844, 681131916905

FDA code information

Use by dates 10/21/13-12/09/13.

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

Full FDA record and distribution details

Original product description

Walmart Deli Potato Salad, Formula PO.121, packaged in 12/16-oz (UPC 681131916783), 6/32-oz (UPC 681131916844) and 6/4-lb (UPC 681131916905) carton cases. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR.

Extracted codes and context

TypeCode / valueContext
UPC681131916783Walmart Deli Potato Salad, Formula PO.121, packaged in 12/16-oz (UPC 681131916783), 6/32-oz (UPC 681131916844) and 6/4-lb (UPC 681131916905) carton cases. Distributed by: Wal-Mart Stores, Inc., Benton
UPC681131916844to Salad, Formula PO.121, packaged in 12/16-oz (UPC 681131916783), 6/32-oz (UPC 681131916844) and 6/4-lb (UPC 681131916905) carton cases. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR.
UPC681131916905aged in 12/16-oz (UPC 681131916783), 6/32-oz (UPC 681131916844) and 6/4-lb (UPC 681131916905) carton cases. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR.

Original FDA recall reason

The recalled products are potentially contaminated with Listeria monocytogenes.

Recall details

Recall number
F-0252-2014
Event ID
66563
FDA status
Terminated
Initiated
Oct 22, 2013
Reported
Jan 1, 2014
Classified
Dec 24, 2013
Terminated
Jan 24, 2017
Quantity
N/A
Location
Beaverton, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distribution was made to AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WI, WV AND WY. Distribution was also made to Canada.

FDA source record · F-0252-2014

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

Follow official FDA and manufacturer guidance.