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H-0636-2025Class III

SUNGAL INC

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
SUNGAL INC
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-10-01
Distribution
The adulterated product was distributed to the following states: CA, MD, NY, VA
Firm state
NJ
Product quantity
29 CASES
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Risk Management & CAPA
Reason for recall

Cyclamate adulteration

Product description

UDK ,Half Plum, 170 g, Container, 24, ambient

Code / lot info

code 2024 12 15 2 UPC 9588837778794

Other recalls SPEQ maps to Risk Management & CAPA
See all Risk Management & CAPA recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →