Light Dry Roasted Unsalted Split Peanuts, Product Code: 400260, packaged in 30 lb. vacuum packed plastic bags placed inside cardboard shipping boxes. The total packaging size is 2100 lbs = 70 x 30 lb boxes.
Class I - DangerousWhat Should You Do?
- Check if you have this product: The following Lot Codes were subject to recall: 7050; 7054; 7128; 7169; 7198; 7270; 7297-7270; 7345; 8029, 8091, 8113, 8158, 8182, 8246, 8308 and 8364.
- 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:
- Pro Nutech Inc.
- Reason for Recall:
- The recalling firm manufactured and distributed peanut products which contained peanuts and/or peanut butter which they received from there bulk peanut supplier, Peanut Corporation of America (PCA). Peanuts and peanut products produced by PCA have been implicated in a recent outbreak of salmonellosis and these product may be contaminated with Salmonella Typhimurium.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Light Dry Roasted Unsalted Split Peanuts, Product Code: 400260, packaged in 30 lb. vacuum packed plastic bags placed inside cardboard shipping boxes. The total packaging size is 2100 lbs = 70 x 30 lb boxes.
Product Codes/Lot Numbers:
The following Lot Codes were subject to recall: 7050; 7054; 7128; 7169; 7198; 7270; 7297-7270; 7345; 8029, 8091, 8113, 8158, 8182, 8246, 8308 and 8364.
Distribution:
Distributed in: KY, UT
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1752-2012
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