RecallHawk
Class III Recall

Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West

Domino Foods Inc

Summary

The FDA issued a Class III for Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), by Domino Foods Inc. Reason: Undeclared Aspartame.

Details

Source

Food Recall

External ID

H-0497-2026

Action Date

2026-02-18

Status

Terminated

Category

food

Product Description

Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041

Lot/Code Info: Lot # 35414, 35416, 35421, 35435

Quantity Affected: 2,023 cases

Reason for Recall

Undeclared Aspartame

Distribution

Product distributed in AR, AZ, CA, IL, KS, KY, LA, MN, MO, MS, NE, NM, TN, TX

Type: Voluntary: Firm initiated

Recall Initiated: 2026-01-13

Company

Domino Foods Inc

West Palm Beach, FL

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Domino Foods Inc has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Domino Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Domino Foods Inc have FDA actions?

Domino Foods Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0497-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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