604293 MEGA OMEGA MIX 12/8 OZ SQ TUB, UPC 2052604293 604293.04 MEGA OMEGA MIX 12/8 OZ SQ TUB BOULDER, UPC 2052604293 604293.05 MEGA OMEGA MIX 12/8 OZ SQ TUB FESTIVAL, UPC 2052604293 604290 MEGA OMEGA MIX 15#, UPC 2052604290 604292 MEGA OMEGA MIX 16/7 OZ - CLAMSHELL,UPC 2052604292 604291 MEGA OMEGA MIX 5#, UPC 2052604291
Class I - DangerousWhat Should You Do?
- Check if you have this product: 11/26/13, 1/11/2014, 1/19/2014,1/11/2014, 1/22/2014, 1/28/2014, 1/29/2014.
- 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:
- Bergin Fruit And Nut Co Inc
- Reason for Recall:
- Bergin Fruit and Nut Company is initiating a recall on a number of pistachio products manufactured using pistachios supplied by ARO Pistachio Inc. Salmonella was found in the environment at the ARO Pistachio Inc. company.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
604293 MEGA OMEGA MIX 12/8 OZ SQ TUB, UPC 2052604293 604293.04 MEGA OMEGA MIX 12/8 OZ SQ TUB BOULDER, UPC 2052604293 604293.05 MEGA OMEGA MIX 12/8 OZ SQ TUB FESTIVAL, UPC 2052604293 604290 MEGA OMEGA MIX 15#, UPC 2052604290 604292 MEGA OMEGA MIX 16/7 OZ - CLAMSHELL,UPC 2052604292 604291 MEGA OMEGA MIX 5#, UPC 2052604291
Product Codes/Lot Numbers:
11/26/13, 1/11/2014, 1/19/2014,1/11/2014, 1/22/2014, 1/28/2014, 1/29/2014.
Distribution:
Distributed in: CA, ID, IL, IN, IA, KS, KY, MI, MN, NV, ND, PA, SD, TN, WI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1738-2013
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