Check the Batch
Class ITerminated in FDA datasetOct 11, 2012

Pierre Peanut Butter & Grape Jelly Cups., 1.50oz. and 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.

Check the codes ↓

The exact product

Pierre Peanut Butter & Grape Jelly Cups., 1.50oz. and 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.

fruit

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

Lot Code: 1070233 (1.50oz) and Lot Codes: 1070485, 2020046, 2030542, 2030818 & 2030819 (2.80oz).

TypeCode / valueContext
lot1070233Lot Code: 1070233 (1.50oz) and Lot Codes: 1070485, 2020046, 2030542, 2030818 & 2030819 (2.80oz).
lot1070485Lot Code: 1070233 (1.50oz) and Lot Codes: 1070485, 2020046, 2030542, 2030818 & 2030819 (2.80oz).
lot2020046Lot Code: 1070233 (1.50oz) and Lot Codes: 1070485, 2020046, 2030542, 2030818 & 2030819 (2.80oz).
lot2030542Lot Code: 1070233 (1.50oz) and Lot Codes: 1070485, 2020046, 2030542, 2030818 & 2030819 (2.80oz).
lot2030818Lot Code: 1070233 (1.50oz) and Lot Codes: 1070485, 2020046, 2030542, 2030818 & 2030819 (2.80oz).

Recall details

Recall number
F-0673-2013
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

FDA source record · F-0673-2013

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.