Class IIITerminatedVoluntary: Firm initiated

Domino Foods Inc: food recall H-0497-2026

Domino Foods Inc of West Palm Beach, FL recalled Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc.,… Reason: Undeclared Aspartame. The FDA listed it as Class III in its Enforcement Report dated Feb 18, 2026; distribution: Arkansas, Arizona, California, Illinois, Kansas, Kentucky, Louisiana, Minnesota, Missouri, Mississippi, Nebraska, New Mexico, Tennessee, Texas.

Record status as published: Terminated (terminated May 27, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041
Product quantity
2,023 cases
Reason for recall
Undeclared Aspartame
Codes, lots and dates on the package
Lot # 35414, 35416, 35421, 35435
Distribution pattern
Product distributed in AR, AZ, CA, IL, KS, KY, LA, MN, MO, MS, NE, NM, TN, TX
Recalling firm
Domino Foods Inc, West Palm Beach, FL
Classification
Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Letter

Dates

EventDate
Recall initiated by the firmJan 13, 2026
Classified by the FDAFeb 11, 2026
Published in the Enforcement ReportFeb 18, 2026
TerminatedMay 27, 2026

Other recalls by Domino Foods Inc

  • H-0637-2025 · Oct 1, 2025 · Class II — Potential contamination with foreign objects.

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0497-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.