FDA recall record

English Bay Batter Schnucks BIG & FLAKY CRESCENT ROLLS, 6 ROLLS, NET WT 11.25 OZ recall — FDA F-0681-2019

Product is being recalled due to undeclared milk in the ingredient list and contains statement.

Class IIclassification
F-0681-2019official record ID
Dec 12, 2018report date

Recall record at a glance

Official recordF-0681-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEnglish Bay Batter L.P.
Report dateDec 12, 2018
Recall initiation dateOct 30, 2018
Quantity336 cases (12 packages/case = 4032 packages)
LocationDelta, N/A, Canada

Official product description

Schnucks BIG & FLAKY CRESCENT ROLLS, 6 ROLLS, NET WT 11.25 OZ UPC 0 41318 57046 5

Why the product was recalled

Product is being recalled due to undeclared milk in the ingredient list and contains statement.

Distribution information

Missouri

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.