CLASS III Food recall · Reported 1 Oct 2025 · FDA Enforcement Report

UDK ,Half Plum, Container, 24, ambient recalled by SUNGAL

SUNGAL is recalling UDK ,Half Plum, Container, 24, ambient, distributed in California, Maryland, New York, Virginia. The recall was initiated on 8 Aug 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codescode 2024 12 15 2 UPC 9588837778794
Quantity recalled29 CASES

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0636-2025
FDA event ID
97491
Recalling firm
SUNGAL, Kearny, NJ
Brand
Udk
Classification
Class III
Status
Terminated
Recall initiated
8 Aug 2025
FDA classified
23 Sep 2025
Reported
1 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Peaches

Timeline

8 Aug 2025Recall initiated by company
23 Sep 2025Classified by FDA+46 days
1 Oct 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Cyclamate adulteration

Product as listed by the FDA

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

Where it was distributed

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

CaliforniaMarylandNew YorkVirginia

Questions about this recall

Why was it recalled?

Cyclamate adulteration

Which lots are affected?

code 2024 12 15 2 UPC 9588837778794

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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