CLASS III Food recall · Reported 15 Oct 2025 · FDA Enforcement Report

Scott & Jon s Honey Sesame Salmon Rice Bowl recalled

Demers Food Group is recalling Scott & Jon s Honey Sesame Salmon Rice Bowl, distributed in 9 states. The recall was initiated on 23 Sep 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesUPC 850016452627, LOT CODE: S235522, BEST IF USED BY: FEB 21 27
Quantity recalled966 cases

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-0046-2026
FDA event ID
97687
Recalling firm
Demers Food Group, Auburn, ME
Brand
Scott
Classification
Class III
Status
Terminated
Recall initiated
23 Sep 2025
FDA classified
14 Oct 2025
Reported
15 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Salmon

Timeline

23 Sep 2025Recall initiated by company
14 Oct 2025Classified by FDA+21 days
15 Oct 2025Published in enforcement report+1 day

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

Product as listed by the FDA

Scott & Jon s Honey Sesame Salmon Rice Bowl

Where it was distributed

Florida, Georgia, Maryland, Massachusetts, Colorado, Washington, California, Illinois, Texas

CaliforniaColoradoFloridaGeorgiaIllinoisMassachusettsMarylandTexasWashington

Questions about this recall

Why was it recalled?

contains undeclared wheat

Which lots are affected?

UPC 850016452627, LOT CODE: S235522, BEST IF USED BY: FEB 21 27

Where was it sold?

Florida, Georgia, Maryland, Massachusetts, Colorado, Washington, California, Illinois, Texas

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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