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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

UDK Half Plum Recalled for Cyclamate Adulteration

Agency Publication Date: September 23, 2025
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Summary

SUNGAL INC is recalling 29 cases of UDK Half Plum (170 g containers) because the product was found to contain cyclamate, an artificial sweetener that is not approved for use in the United States. This recall involves products with UPC 9588837778794 and production codes marked as 2024 12 15 2. Consumers who have purchased these plums should not eat them and are advised to return the product to the store where it was bought for a full refund.

Risk

The product is adulterated with cyclamate, which is an unapproved sweetener in the United States. Consuming products with unapproved food additives can pose potential health risks to consumers.

What You Should Do

  1. This recall affects UDK Half Plum sold in 170 g containers with UPC 9588837778794 and code 2024 12 15 2.
  2. Check the container for the lot number 2024 and the specific production code 2024 12 15 2 to determine if your product is part of the recall.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact SUNGAL INC directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional assistance.

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: UDK Half Plum (170 g)
Variants: Ambient
UPC Codes:
9588837778794
Lot Numbers:
2024
2024 12 15 2

Packaged 24 containers per case.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97491
Status: Resolved
Manufacturer: SUNGAL INC
Manufactured In: United States
Units Affected: 29 CASES
Distributed To: California, Maryland, New York, Virginia

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.