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Class ITerminated in FDA datasetRecall initiated Feb 3, 2009

B. A. Sweetie Chocolate Bridge Mix in plastic bags 2 lb

Recalling firm: BA Sweetie Candy Co

Why it was recalled

Product is being recalled because it was manufactured using peanut products recalled by Peanut Corporation of America. The peanut products has the potential to be contaminated…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 11, 2013.

Check your package

Compare the exact product and package details with the label you have.

ProductB. A. Sweetie Chocolate Bridge Mix in plastic bags 2 lb, UPC 0 17598 90609 6, 5 lb, UPC 0 17598 00609 3; & Dave's Markets Chocolate Bridge Mix in plastic bags, 4 oz, UPC 017598 70609 2.
Package size2 lb
UPC017598006093, 017598706092, 017598906096

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

B. A. Sweetie Chocolate Bridge Mix in plastic bags 2 lb, UPC 0 17598 90609 6, 5 lb, UPC 0 17598 00609 3; & Dave's Markets Chocolate Bridge Mix in plastic bags, 4 oz, UPC 017598 70609 2.

Extracted codes and context

TypeCode / valueContext
UPC017598006093eetie Chocolate Bridge Mix in plastic bags 2 lb, UPC 0 17598 90609 6, 5 lb, UPC 0 17598 00609 3; & Dave's Markets Chocolate Bridge Mix in plastic bags, 4 oz, UPC 017598 70609 2.
UPC01759870609217598 00609 3; & Dave's Markets Chocolate Bridge Mix in plastic bags, 4 oz, UPC 017598 70609 2.
UPC017598906096B. A. Sweetie Chocolate Bridge Mix in plastic bags 2 lb, UPC 0 17598 90609 6, 5 lb, UPC 0 17598 00609 3; & Dave's Markets Chocolate Bridge Mix in plastic bags, 4 oz, UPC 017598 70609 2.

Original FDA recall reason

Product is being recalled because it was manufactured using peanut products recalled by Peanut Corporation of America. The peanut products has the potential to be contaminated with Salmonella

Recall details

Recall number
F-1039-2013
Event ID
51892
FDA status
Terminated
Initiated
Feb 3, 2009
Reported
Mar 13, 2013
Classified
Mar 1, 2013
Terminated
Mar 11, 2013
Quantity
72 bags
Location
Brooklyn, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

The product was distributed to one customer in Ohio.

FDA source record · F-1039-2013

Data updated September 16, 2026. View official FDA data ↗

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