Class I Recall

The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 78

Summary

The FDA issued a Class I for The Tuna Salad product container is mislabeled with a Chicken Salad lid, which s by Reser's Fine Foods, Inc.. Reason: Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad..

Details

Source

Food Recall

External ID

H-0517-2026

Action Date

2026-02-25

Status

Terminated

Product Description

The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed by US Foods, Inc. Rosemont, IL 60018. The lid declares Contains: Eggs, Milk, Wheat. The immediate 5-lb tub has no side labeling (besides the lid). The master cardboard case label is correct and states: Molly Kitchen's Tuna Salad, (item #) 794599, 2/5 LB tubs per case, Net Wt. 10 LB (4.53 kg). UPC 075810876447. Distributed by US Foods, Inc. Rosemont, IL 60018. Contains: Egg, Wheat, Fish (Tuna).

Lot/Code Info: Lot 1410100754 Use By FEB/21/26

Quantity Affected: 149 cases (2 tubs /case) or 298 total tubs

Reason for Recall

Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.

Distribution

Distributed in AZ, CA, NV, UT and WA.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-01-30

Company

Reser's Fine Foods, Inc.

Beaverton, OR

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Reser's Fine Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Reser's Fine Foods, Inc. have FDA actions?

Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0517-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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