FDA recall record

Gonnella Frozen Products Brat Roll Frozen Dough Product Code 18429 UPC: 00078296184292 recall — FDA F-0973-2023

Undeclared egg

Class Iclassification
F-0973-2023official record ID
Jun 14, 2023report date

Recall record at a glance

Official recordF-0973-2023
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmGonnella Frozen Products, LLC
Report dateJun 14, 2023
Recall initiation dateMay 15, 2023
Quantity949 cases
LocationHazle Township, PA, United States

Official product description

Brat Roll Frozen Dough Product Code 18429 UPC: 00078296184292. Individual unit wt 2.50 oz. Packaged in a cardboard box. 180 pieces per case.

Why the product was recalled

Undeclared egg

Distribution information

Distributed to distributors in MI, MN, OH, UT, and CA.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.