Dean Foods Albertsons Peanut Butter Chocoate Ice Cream Recall

Why it was recalled

Product was manufactured using an ingredient that was recalled due to Salmonella contamination.

Product description

Albertsons Peanut Butter Chocoate Ice Cream, 1.5 QTS (1.42 L), (chocolate ice cream with a peanut butter swirl)

Lot numbers, UPCs & expiration codes

UPC 41163 45903, any Best By or EXP dates ranging from 3/26/2011 to 8/03/2013, Plant Code 49-11 or 06-20.

Where it was sold

Sold by retailers in AZ, CA, CO, ID, MT, ND, NV, OR, UT, WA, and WY.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-0686-2013
Classification: Class I
Status: Terminated
Recall initiated: Oct 10, 2012
FDA report date: Nov 21, 2012
Quantity: 67,781 x 1.5 QTS
Recall type: Voluntary: Firm initiated
Recalling firm: Dean Foods Company

Original FDA data

Every field from FDA enforcement report F-0686-2013, exactly as published.

Show all FDA fields

City: Dallas
State: TX
Status: Terminated
Country: United States
Event ID: 63480
Address: 3114 S Haskell Ave
Address (line 2): 4727 Sapphire St.
Code information: UPC 41163 45903, any Best By or EXP dates ranging from 3/26/2011 to 8/03/2013, Plant Code 49-11 or 06-20.
Postal code: 75223-3100
Report date: Nov 21, 2012
Product type: Food
Recall number: F-0686-2013
Classification: Class I
Recalling firm: Dean Foods Company
Product quantity: 67,781 x 1.5 QTS
Termination date: Dec 31, 2012
Reason for recall: Product was manufactured using an ingredient that was recalled due to Salmonella contamination.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Albertsons Peanut Butter Chocoate Ice Cream, 1.5 QTS (1.42 L), (chocolate ice cream with a peanut butter swirl)
Distribution pattern: Sold by retailers in AZ, CA, CO, ID, MT, ND, NV, OR, UT, WA, and WY.
Recall initiation date: Oct 10, 2012
Initial firm notification: Press Release
Center classification date: Nov 13, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0686-2013, published Nov 21, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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