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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Packaged & Processed

Haiyue Food Preserved Vegetable Recalled for Unapproved Cyclamate

Agency Publication Date: March 17, 2023
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Summary

XIUMIN LIN is recalling 55 boxes of Haiyue Food Nutritional Preserved Vegetable because they contain cyclamate, an artificial sweetener that is not approved for use in the United States. The affected products are labeled with the date 2021/12/25 and UPC 6921821000663. No illnesses or incidents have been reported in connection with this product to date. Consumers who have purchased this item should return it to the store for a refund or dispose of it.

Risk

The product contains cyclamate, a sweetener that is not permitted for use in food products sold in the U.S. markets.

What You Should Do

  1. This recall involves Haiyue Food Nutritional Preserved Vegetable labeled with the date 2021/12/25 and UPC 6921821000663.
  2. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Haiyue Food Nutritional Preserved Vegetable
UPC Codes:
6921821000663
Lot Numbers:
2021/12/25

Recall Number: F-0624-2023; Quantity affected: 55 boxes.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91640
Status: Resolved
Manufacturer: XIUMIN LIN
Manufactured In: United States
Units Affected: 55 boxes
Distributed To: New York, North Carolina, Florida, Indiana

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. 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. Refer to the openFDA terms of service for more information.