FDA recall record

Toft Dairy Prime Time brand Buckeye Bites Ice Cream in a paper carton 48 recall — FDA F-0683-2013

Product was manufactured using an ingredient that was recalled due to Salmonella contamination.

Class Iclassification
F-0683-2013official record ID
Nov 21, 2012report date

Recall record at a glance

Official recordF-0683-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmToft Dairy Inc.
Report dateNov 21, 2012
Recall initiation dateOct 9, 2012
Quantity15,600-48oz cartons and 1,482 3 gallon tubs
LocationSandusky, OH, United States

Official product description

Prime Time brand Buckeye Bites Ice Cream in a paper carton 48 oz containers and 3 gallon tubs

Why the product was recalled

Product was manufactured using an ingredient that was recalled due to Salmonella contamination.

Distribution information

3 Distributors 211 Retailers

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.