FDA Food recall ·

Reser's Gourmet Tuna Salad, net wt recall

This is an FDA Class I recall — the most serious type.

Recall number
H-0541-2025
Date
(initiated July 16, 2025)
Company / brand
Reser's Fine Foods, Inc.
15570 SW Jenkins Rd, Beaverton, OR, United States
Category
Food › Class I
Classification
Class I
Status
Terminated
Units affected
240 cases
Hazard tags
Listeria Microbial contamination
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

Reser's Gourmet Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with white lid with white sticker. Keep Refrigerated. Distributed by Reser's Fine Foods, Beaverton, OR. UPC on 5lb. TUB: 71117 85506 GTIN on Master Case (2/5# per case): 1007111785506

Why was it recalled?

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

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

Lot 1420043324 Use By: AUG/17/25 Lot 1420046644 Use By: AUG/24/25

Distribution

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.

States: Arkansas Colorado Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri Mississippi North Dakota Nebraska New Hampshire New Jersey New Mexico New York Ohio Oklahoma Pennsylvania Tennessee Texas Virginia Wisconsin

What does Class I mean?

Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.

Source: FDA (food), recall H-0541-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.