B. A. Sweetie Double Dip Peanuts in plastic bags 2 lb
Recalling firm: BA Sweetie Candy Co
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.
017598006871, 017598706870, 017598906874Match 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 Double Dip Peanuts in plastic bags 2 lb, UPC 0 17598 90687 4, 5 lb, UPC 0 17598 00687 1; & Dave's Market Chocolate Double Dip Peanuts in plastic bags, 4 oz, UPC 017598 70687 0
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 017598006871 | Sweetie Double Dip Peanuts in plastic bags 2 lb, UPC 0 17598 90687 4, 5 lb, UPC 0 17598 00687 1; & Dave's Market Chocolate Double Dip Peanuts in plastic bags, 4 oz, UPC 017598 70687 0 |
| UPC | 017598706870 | 0687 1; & Dave's Market Chocolate Double Dip Peanuts in plastic bags, 4 oz, UPC 017598 70687 0 |
| UPC | 017598906874 | B. A. Sweetie Double Dip Peanuts in plastic bags 2 lb, UPC 0 17598 90687 4, 5 lb, UPC 0 17598 00687 1; & Dave's Market Chocolate Double Dip Peanuts in plastic bags, 4 oz, UPC 017598 70687 0 |
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-1038-2013
- Event ID
- 51892
- FDA status
- Terminated
- Initiated
- Feb 3, 2009
- Reported
- Mar 13, 2013
- Classified
- Mar 1, 2013
- Terminated
- Mar 11, 2013
- Quantity
- 168/4 oz plastic 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.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.