FDA recall record

Bake One Pre Proof Danish Net Wt: 13.7lbs recall — FDA F-0407-2019

The firm found what appeared to be plastic in the product.

Class IIclassification
F-0407-2019official record ID
Nov 14, 2018report date

Recall record at a glance

Official recordF-0407-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBake One, Inc.
Report dateNov 14, 2018
Recall initiation dateOct 5, 2018
Quantity378 cs/44/5 oz Danish
LocationSmyrna, GA, United States

Official product description

Pre Proof Danish Net Wt: 13.7lbs (6.2Kg) Contains: Eggs, Milk, Soy and Wheat KEEP FROZEN AT 0 F OR BELOW Bake One, Inc. Smyrna, GA 30082 UPC 8 10509 01152 6

Why the product was recalled

The firm found what appeared to be plastic in the product.

Distribution information

Product was shipped to the following states: GA, IN, LA, MN, MO, NC, OH, OK, TX & WY.

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: Telephone.

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.