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Class III: unlikely to cause harmTerminated

Sungal Udk Recall

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

SUNGAL INC · Kearny, NJ

Risk level
Class III
Reported by FDA
Oct 1, 2025
Recall ID
H-0636-2025
Check your lot numberHow we source this data

Summary

Sungal recalled Udk starting Aug 8, 2025. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report H-0636-2025 on Oct 1, 2025. Reason: Cyclamate adulteration. Status: Terminated.

Why it was recalled

Cyclamate adulteration

Product description

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

Lot numbers, UPCs & expiration codes

code 2024 12 15 2 UPC 9588837778794

Where it was sold

The adulterated product was distributed to the following states: CA, MD, NY, VA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0636-2025
Classification
Class III
Status
Terminated
Recall initiated
Aug 8, 2025
FDA report date
Oct 1, 2025
Quantity
29 CASES
Recall type
Voluntary: Firm initiated
Recalling firm
SUNGAL INC

Original FDA data

Every field from FDA enforcement report H-0636-2025, exactly as published.

Show all FDA fields
City
Kearny
State
NJ
Status
Terminated
Country
United States
Event ID
97491
Address
69 Sellers St # 81
Code information
code 2024 12 15 2 UPC 9588837778794
Postal code
07032-4227
Report date
Oct 1, 2025
Product type
Food
Recall number
H-0636-2025
Classification
Class III
Recalling firm
SUNGAL INC
Product quantity
29 CASES
Termination date
Dec 8, 2025
Reason for recall
Cyclamate adulteration
Voluntary / mandated
Voluntary: Firm initiated
Product description
UDK ,Half Plum, 170 g, Container, 24, ambient
Distribution pattern
The adulterated product was distributed to the following states: CA, MD, NY, VA
Recall initiation date
Aug 8, 2025
Initial firm notification
E-Mail
Center classification date
Sep 23, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0636-2025, published Oct 1, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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