Home / Food recalls / 2012
Dean Foods of California Inc
FDA recall F-0564-2013 · Class I · reported 2012-11-07 · Terminated
- Product
- Albertsons Brand Peanut Butter Cup Ice Cream, 1.5 Quarts (1.42L), commonly called a 48 fl oz container. Peanut Butter Cup Ice Cream, (Vanilla ice cream with peanut butter cup pieces, fudge and peanut butter swirls); 1.5 QTS (1.42L), (UPC Code 0 41163 45891 8 for Albertsons Peanut Butter Cup) Packaged in paper cardboard round oblong container. Labeled with a. Buena Park (IMS Plant Number 06-20). Labeled as "Distributed by SUPERVALU INC. Eden Prairie, MN 55344". 06-20 1024 RA (plant code, 24 hour time, operator initial) MFG 10/08/12 EXP 10/08/13 LOTE A (manufacturing month, day, year , expiration month, day, year, lot number) Code date is injected on the bottom of container in black ink UPC Code: 0 41163 45891 8 for Albertsons Peanut Butter Cup
- Reason
- This recall was initiated because the affected products contain a peanut butter ingredient supplied by Sunland, Inc. which may be contaminated with Salmonella. The peanut butter manufacturer Sunland recently expanded its nationwide product recall.
- Quantity
- 157,110 units
- Distribution
- California, Idaho, Montana, Nevada, North Dakota, Oregon, Utah, Wyoming, Washington.
- Firm location
- CA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Recall started
- 2012-10-10
- Terminated
- 2013-08-28
- Code info
- Buena Park (IMS Plant Number 06-20) 06-20 1024 RA (plant code, 24 hour time, operator initial) MFG 10/08/12 EXP 10/08/13 LOTE A (manufacturing month, day, year , expiration month, day, year, lot number) Code date is injected on the bottom of container in black ink. UPC Code: 0 41163 45903 8 for Albertsons Peanut Butter Chocolate and 0 41163 45891 8 for Albertsons Peanut Butter Cup
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.