RecallHawk
Class I Recall

Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628

ZB Importing LLC

Summary

The FDA issued a Class I for Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 86905 by ZB Importing LLC. Reason: Undeclared wheat and egg.

Details

Source

Food Recall

External ID

F-0633-2025

Action Date

2025-03-19

Status

Terminated

Category

food

Product Description

Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628

Lot/Code Info: L07 EXP 06/2025 and L09 EXP 9/2025

Quantity Affected: 1881 Cases

Reason for Recall

Undeclared wheat and egg

Distribution

Products were distributed through retail stores in Ontario, Canada and the following US states AL, AR, CA, CT, CO, DC, DE, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NE, NC, NH, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, VA, WA, WI and WV.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-02-15

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.

ZB Importing LLC has 8 FDA actions in our database, including 8 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ZB Importing LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does ZB Importing LLC have FDA actions?

ZB Importing LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0633-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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