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 - Dangerous

What Should You Do?

  1. 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.
  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:
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.gov

FDA Recall Number: F-1738-2013

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