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Class IFDA · February 25, 2026

The Tuna Salad product container is mislabeled with a recall

Recalled by Reser's Fine Foods, Inc.

The product, as the FDA describes it: 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).

Why it was recalled

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

The FDA has since closed this recall out, which means the company finished removing the product from sale. It is kept here because a closed recall still matters to anyone holding a package bought before it ended.

What to do if you have it

This is a labelling failure rather than spoiled food, so it matters entirely to whoever eats it. If nobody in your household reacts to what went undeclared here, the product is not dangerous to you, though you can still return it. If somebody does, treat every package from the affected run as unsafe no matter how much has already been eaten without incident.

How to tell whether your package is one of them

A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.

Lot 1410100754 Use By FEB/21/26

The details on record

Recalling companyReser's Fine Foods, Inc.
Company locationBeaverton, OR
Where it was distributedDistributed in AZ, CA, NV, UT and WA.
How much was recalled149 cases (2 tubs /case) or 298 total tubs
Recall startedJanuary 30, 2026
Published by the FDAFebruary 25, 2026
Recall typeVoluntary: Firm initiated
How the company announced itLetter
FDA recall numberH-0517-2026

Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.

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