PB & Grape Jamwich, 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
Recalling firm: Advance Pierre N
Why it was recalled
Products were manufactured with peanut butter products recalled by Sunland, Inc. found to be contaminated with Salmonella.
The exact product
PB & Grape Jamwich, 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, 5/19/12, 4/15/12, 4/28/12, 5/28/12, 5/27/12, 6/5/12, 12/4/12 & 1/7/13.
| Type | Code / value | Context |
|---|---|---|
| lot | 1070180 | UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, |
| lot | 1070181 | UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. date |
| lot | 1070316 | UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/1 |
| lot | 1070466 | UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/1 |
| lot | 1070467 | UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/1 |
| lot | 1070468 | UPC Code: 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12 |
| lot | 1070469 | : 75999613968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, |
| lot | 1070547 | 3968, Lot Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, |
| lot | 1080048 | Codes: 1070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, 5/19/12, |
| lot | 1080305 | 070180, 1070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, 5/19/12, 4/15/12, |
| lot | 1080570 | 070181, 1070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, 5/19/12, 4/15/12, 4/28/12, |
| lot | 1090087 | 070316, 1070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, 5/19/12, 4/15/12, 4/28/12, 5/28/12, |
| lot | 2020071 | 070466, 1070467, 1070468, 1070469, 1070547, 1080048, 1080305, 1080570, 1090087, 2020071 & 2020629, Exp. dates: 4/27/12, 4/26/12, 4/13/12, 5/7/12, 5/8/12, 5/20/12, 5/19/12, 4/15/12, 4/28/12, 5/28/12, 5/27/12, |
Recall details
- Recall number
- F-0670-2013
- Event ID
- 63448
- FDA status
- Terminated
- Initiated
- Oct 11, 2012
- Reported
- Nov 21, 2012
- Classified
- Nov 9, 2012
- Terminated
- Feb 12, 2013
- Quantity
- 3.2 Million lbs. (total for all products)
- Location
- Wooster, 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
U.S. Nationwide
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.