FDA Food recall ·
Reser's Tuna Salad, net wt recall
This is an FDA Class I recall — the most serious type.
- Recall number
- H-0540-2025
- 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
- 173 cases
- Hazard tags
- Listeria Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep Refrigerated. This item does not contain ingredient Pickle Relish. Distributed by Reser's Fine Foods, Beaverton, OR. UPC on 5lb. TUB: 71117 14138 GTIN on Master Case (2/5# per case): 1007111714138
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 1420043945 Use By: AUG/26/25
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-0540-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.