FDA recall record

ZB Importing Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic recall — FDA F-0631-2025

Undeclared egg

Class Iclassification
F-0631-2025official record ID
Mar 19, 2025report date

Recall record at a glance

Official recordF-0631-2025
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmZB Importing LLC
Report dateMar 19, 2025
Recall initiation dateFeb 15, 2025
Quantity2289 cases
LocationCicero, IL, United States

Official product description

Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473

Why the product was recalled

Undeclared egg

Distribution information

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.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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