Class ITerminated in FDA datasetRecall initiated Jul 16, 2025

Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli.…

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.

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 26, 2026.

Check your package

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

ProductSignature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in clear plastic tub with printed white lid. Keep Refrigerated. Distributed by Lucerne Foods, PO Box 99, Pleasanton, CA. UPC on 3lb. TUB: 71117 06036 GTIN on Master Case (2/3# per case): 10071117060369
Package size3lb

FDA code information

Lot 1420043298 Use By: AUG/17/25 Lot 1420047265 Use By: AUG/24/25

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

Full FDA record and distribution details

Original product description

Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in clear plastic tub with printed white lid. Keep Refrigerated. Distributed by Lucerne Foods, PO Box 99, Pleasanton, CA. UPC on 3lb. TUB: 71117 06036 GTIN on Master Case (2/3# per case): 10071117060369

Original FDA recall reason

Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.

Recall details

Recall number
H-0539-2025
Event ID
97283
FDA status
Terminated
Initiated
Jul 16, 2025
Reported
Aug 20, 2025
Classified
Aug 27, 2025
Terminated
Feb 26, 2026
Quantity
165 cases
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

Distributed in AR, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, ND, NE, NH, NJ, NM, NY, OH, OK, PA, TN, TX, VA, and WI.

FDA source record · H-0539-2025

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

Follow official FDA and manufacturer guidance.