Label reads in part "***CASCADE GLACIER CHOCOLATE PEANUT BUTTER ***3 GALLONS (11.36 l) Plant 41-90 DISTRIBUTED BY OREGON ICE CREAM CO. EUGENE OR 97402" upc 0 72609 60082 0.

Class I - Dangerous
Recalled: September 27, 2012 Oregon Ice Cream Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    12223A recall expansion includes lots 10012, 10062, 10088, 10144, 10209, 10243, 10271, 10314, 11021A, 11039A, 11054A, 11067A, 11101A, 11150B, 11173B, 11209B, 11256A, 11319A, 11353A, 12044A, 12073A, 12105B, 12137A, 12168A, 12223A
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Oregon Ice Cream, LLC
Reason for Recall:
The products are being recalled because they contain peanut butter associated with the Sunland, Inc. recall and have the potential to be contaminated with Salmonella.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Label reads in part "***CASCADE GLACIER CHOCOLATE PEANUT BUTTER ***3 GALLONS (11.36 l) Plant 41-90 DISTRIBUTED BY OREGON ICE CREAM CO. EUGENE OR 97402" upc 0 72609 60082 0.

Product Codes/Lot Numbers:

12223A recall expansion includes lots 10012, 10062, 10088, 10144, 10209, 10243, 10271, 10314, 11021A, 11039A, 11054A, 11067A, 11101A, 11150B, 11173B, 11209B, 11256A, 11319A, 11353A, 12044A, 12073A, 12105B, 12137A, 12168A, 12223A

Distribution:

Distributed in: AK, CA, CO, CT, IA, ID, IL, IN, MA, MC, NH, NY, OR, PA, WA, FL, TX, DE, GA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0318-2013

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