SUNGAL INC is recalling specific lots of UDK Half Plum in 170-gram containers because they contain cyclamate, which constitutes an adulteration. The affected products were distributed to California, Maryland, New York, and Virginia. No remedy or injury information is provided in the record. Read more at govinfonow.com/recall/7368-udk-half-plum-recall-cyclamate-adulteration-in-170g-containers.
“UDK Half Plum Recall: Cyclamate Adulteration in 170g Containers.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/7368-udk-half-plum-recall-cyclamate-adulteration-in-170g-containers. Based on FDA recall #H-0636-2025.
The FDA announced on August 8, 2025, that SUNGAL INC voluntarily recalled UDK Half Plum products due to cyclamate adulteration. The Class III recall affects 29 cases distributed in California, Maryland, New York, and Virginia.
How to tell if you have it
UDK Half Plum 170 g Container
UPC 09588837778794
Code 2024 12 15
The hazard
The product is adulterated with cyclamate, a banned sweetener. The FDA classified the recall as Class III.
Context
GovInfoNow's records show SUNGAL INC has one other recall on record since February 12, 2026, involving undeclared food dyes in Jelly Snacks. Other recent recalls of similar products include Olive Skewers with Cyclamates Recalled (November 13, 2025), Mei Heong Yuen Peanuts Recalled for Banned Cyclamates (February 19, 2026), and Dadi Nongfu Dried Salt Chili Vegetables Recall (November 13, 2025).
How to tell if you have this one
Look for UDK Half Plum in a 170 g container with code 2024 12 15 and UPC 9588837778794. The product was distributed to CA, MD, NY, and VA.
Brand
UDK
Product
UDK ,Half Plum, 170 g, Container, 24, ambient
Category
Food
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “The adulterated product was distributed to the following states: CA, MD, NY, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Maryland, New York, Virginia.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0636-2025 (August 8, 2025)
Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
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