HIGHFDA FOOD

SUNGAL UDK Half Plum 170 g Recall for Cyclamate Adulteration (2025)

SUNGAL Inc. recalls 29 cases of UDK Half Plum, 170 g containers distributed to California, Maryland, New York and Virginia. The product is adulterated with cyclamate. Consumers should not consume it and should email SUNGAL Inc. for refund or replacement information.

Official notice
SUNGALFood & Beveragescode 2024 12 15 2 UPC 9588837778794

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA FOOD
Recall date
August 8, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
August 8, 2025
Hazard Level
HIGH
Brand
SUNGAL
Category
Food & Beverages
Sold At
Unknown
Geographic Scope
4 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
SUNGAL
Product type
Plum halves in 170 g containers
Model numbers
code 2024 12 15 2 UPC 9588837778794
Sizes
170 g
Sold at
Unknown
Where affected
CA, MD, NY, VA

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 8, 2025

  2. Reported by FDA FOOD

    October 1, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Cyclamate adulteration

What You Should Do

Consumers who have purchased this product should not consume it. Contact SUNGAL INC for refund or replacement information. Notification method: E-Mail

About This Product

UDK Half Plum is a 170 g fruit product packaged in 24-count cases. It is marketed as a ready-to-eat plum product.

Why This Is Dangerous

The product contains cyclamate adulteration, an unauthorized sweetener. The health impact is not detailed in the recall, but consumers are advised not to consume the product.

Industry Context

This recall is not described as part of a broader industry pattern.

Practical Guidance

How to identify if yours is affected

  1. Check for label SUNGAL UDK Half Plum 170 g
  2. Confirm code 2024 12 15 2 on packaging

Where to find product info

UPC on the back of the container, date code on the lid or label, packaging

What timeline to expect

Refund or replacement processing timelines not specified in the recall

If the manufacturer is unresponsive

  • Document all contact attempts with SUNGAL INC
  • File a consumer-protection complaint if issues persist
  • Consider contacting FDA recall line for guidance

How to prevent similar issues

  • Buy from reputable retailers
  • Check packaging integrity and date codes before purchase
  • Look for recall notices on FDA enforcement pages and manufacturer sites

Documentation advice

Keep the packaging, purchase receipts, and all recall correspondence; take photos of the product and UPC/date code

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Product Details

Model codes: code 2024 12 15 2; UPC 9588837778794. Sold in: CA, MD, NY, VA. Sold from: Unknown. Quantity: 29 CASES. Size: 170 g per container; 24 containers per case. Price: Unknown.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Distributed to CA, MD, NY, VA
  • Cyclamate adulteration detected
  • Consumers should not consume; contact SUNGAL for refund or replacement

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
POISONINGOTHER

Product Details

Brand
Model Numbers
code 2024 12 15 2 UPC 9588837778794
Affected States
CA, MD, NY, VA
Report Date
October 1, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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