CLASS II Food recall · Reported 10 Sep 2025 · FDA Enforcement Report

Red Bliss Potato Salad recalled by Hans Kissle Company

Hans Kissle Company is recalling Red Bliss Potato Salad, distributed in Connecticut, Massachusetts, New Jersey, New York, Rhode Island. The recall was initiated on 4 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPC Code 036217673706 and Use By: 8/20/25 and 9/25/25
Quantity recalled66 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0558-2025
FDA event ID
97392
Recalling firm
Hans Kissle Company, Haverhill, MA
Classification
Class II
Status
Terminated
Recall initiated
4 Aug 2025
FDA classified
3 Sep 2025
Reported
10 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Product category
Salad Kits

Timeline

4 Aug 2025Recall initiated by company
3 Sep 2025Classified by FDA+30 days
10 Sep 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Contains undeclared wheat. The top label identifies the product as potato salad, but the unit contains pasta salad.

Product as listed by the FDA

Hans Kissle Red Bliss Potato Salad

Where it was distributed

MA, RI, CT, NJ, and NY

ConnecticutMassachusettsNew JerseyNew YorkRhode Island

Questions about this recall

Why was it recalled?

Contains undeclared wheat. The top label identifies the product as potato salad, but the unit contains pasta salad.

Which lots are affected?

UPC Code 036217673706 and Use By: 8/20/25 and 9/25/25

Where was it sold?

MA, RI, CT, NJ, and NY

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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