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DEMERS FOOD GROUP LLC Recall: contains undeclared wheat

United States

TerminatedClass III

Company
DEMERS FOOD GROUP LLC
Product
Scott & Jon s Honey Sesame Salmon Rice Bowl
Recall date
September 23, 2025
Terminated
April 20, 2026
Source
FDA

Reason for recall

contains undeclared wheat

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Scott & Jon s Honey Sesame Salmon Rice Bowl Not published in this source record 966 cases UPC 850016452627, LOT CODE: S235522, BEST IF USED BY: FEB 21 27

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0046-2026
Event ID
97687
Status
Terminated
Classification
Class III
Company
DEMERS FOOD GROUP LLC
Product description
Scott & Jon s Honey Sesame Salmon Rice Bowl
Quantity
966 cases
Reason
contains undeclared wheat
Recall initiation date
September 23, 2025
Report date
October 15, 2025
Classification date
Not published in this source record
Termination date
April 20, 2026
Distribution pattern
Florida, Georgia, Maryland, Massachusetts, Colorado, Washington, California, Illinois, Texas
UPC, lot, and code information
UPC 850016452627, LOT CODE: S235522, BEST IF USED BY: FEB 21 27
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: DEMERS FOOD GROUP LLC

Other recalls from DEMERS FOOD GROUP LLC

FDA Recall United States Terminated Historical recordClass I

DEMERS FOOD GROUP LLC

Product
Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Published
October 29, 2025
Distribution
Nationwide

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.