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Class II: temporary or reversible health riskTerminated

Sungal Xzl Recall

XZL, Jelly Snacks, 12

SUNGAL INC · Kearny, NJ

Risk level
Class II
Reported by FDA
May 13, 2026
Recall ID
H-0689-2026
Check your lot numberHow we source this data

Summary

Sungal recalled Xzl starting Feb 12, 2026. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0689-2026 on May 13, 2026. Reason: Product Contains undeclared FD&C Yellow #5 & #6 and Red #40. Status: Terminated.

Why it was recalled

Product Contains undeclared FD&C Yellow #5 & #6 and Red #40

Product description

XZL, Jelly Snacks, 12.68 OZ, Bag. 12 Bags per Case.

Lot numbers, UPCs & expiration codes

UPC CODE 6926475202449

Where it was sold

The product was distributed to the following states : NY, RI

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-0689-2026
Classification
Class II
Status
Terminated
Recall initiated
Feb 12, 2026
FDA report date
May 13, 2026
Quantity
100 Cases
Recall type
Voluntary: Firm initiated
Recalling firm
SUNGAL INC

Original FDA data

Every field from FDA enforcement report H-0689-2026, exactly as published.

Show all FDA fields
City
Kearny
State
NJ
Status
Terminated
Country
United States
Event ID
98570
Address
69 Sellers St # 81
Code information
UPC CODE 6926475202449
Postal code
07032-4227
Report date
May 13, 2026
Product type
Food
Recall number
H-0689-2026
Classification
Class II
Recalling firm
SUNGAL INC
Product quantity
100 Cases
Termination date
May 28, 2026
Reason for recall
Product Contains undeclared FD&C Yellow #5 & #6 and Red #40
Voluntary / mandated
Voluntary: Firm initiated
Product description
XZL, Jelly Snacks, 12.68 OZ, Bag. 12 Bags per Case.
Distribution pattern
The product was distributed to the following states : NY, RI
Recall initiation date
Feb 12, 2026
Initial firm notification
E-Mail
Center classification date
May 4, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0689-2026, published May 13, 2026. View the source record (openFDA) · FDA enforcement reports

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

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