Product is 50 lb Bag Peanut Butter. Product Case is labeled in part: "***50 Lbs Bag***PEANUT BUTTER***PRODUCT OF USA*** 50 Lb Bag Lot 113112 - 225 boxes shipped to Cheney Brothers, Ocala, FL. ----------- 10/5 Lbs Bag Peanut Butter. Product Case is labeled in part: "***10/5 Lbs Bag PEANUT BUTTER***PRODUCT OF USA***" 10 / 5 Lb Bags Lot 113112 - 48 boxes shipped to Cheney Brothers, Ocala, FL.
Class I - DangerousWhat Should You Do?
- Check if you have this product: lot code: 113112.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- Sunshine Peanut Company
- Reason for Recall:
- On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Product is 50 lb Bag Peanut Butter. Product Case is labeled in part: "***50 Lbs Bag***PEANUT BUTTER***PRODUCT OF USA*** 50 Lb Bag Lot 113112 - 225 boxes shipped to Cheney Brothers, Ocala, FL. ----------- 10/5 Lbs Bag Peanut Butter. Product Case is labeled in part: "***10/5 Lbs Bag PEANUT BUTTER***PRODUCT OF USA***" 10 / 5 Lb Bags Lot 113112 - 48 boxes shipped to Cheney Brothers, Ocala, FL.
Product Codes/Lot Numbers:
lot code: 113112.
Distribution:
Distributed in: CA, FL, NJ, WA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0118-2013
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