Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473
Summary
The FDA issued a Class I for Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC by ZB Importing LLC. Reason: Undeclared egg.
Details
Source
Food Recall
External ID
F-0631-2025
Action Date
2025-03-19
Status
Terminated
Category
food
Product Description
Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473
Lot/Code Info: L03 EXP 03/2025, L05 EXP 05/2025, L09 EXP 09/2025 and L11 EXP 11/2025
Quantity Affected: 2289 cases
Reason for Recall
Undeclared 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
Cicero, IL
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-0631-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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