Recall record at a glance
| Official record | F-0564-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Dean Foods of California Inc. |
| Report date | Nov 7, 2012 |
| Recall initiation date | Oct 10, 2012 |
| Quantity | 157,110 units |
| Location | Buena Park, CA, United States |
Official product description
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
Why the product was recalled
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.
Distribution information
California, Idaho, Montana, Nevada, North Dakota, Oregon, Utah, Wyoming, Washington.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.