Salsa / Nachos Meal with Red Vegetable, Item # 61419

Class I - Dangerous
Recalled: May 19, 2016 E S Foods Produce

What Should You Do?

  1. Check if you have this product:
    Lot #'s: 1) 5322, 2) 6004, 3) 6039, 4) 6046, 5) 6057, 6) 6074, 7) 6090, 8) 6116, 9) 6124, 10) 6127, 11) 6130, 12) 6137, 13) 6146, 14) 6639, 15) 6646 Best Used By: 1) 5/21/16, 2) 7/8/16, 3) 7/17/16 & 9/16/16, 4) 9/22/16, 5) 9/2/16 & 9/22/16, 6) 10/28/16, 7) 12/1/16, 8) 12/1/16 & 12/16/16, 9) 12/1/16, 10) 10/30/16, 11) 12/1/16, 12) 12/1/16 & 12/14/16, 13) 9/22/16, 14) 7/17/16, 15) 9/22/16
  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:
E S Foods
Reason for Recall:
A potential for Listeria monocytogenes contamination was verified by the sunflower kernel raw material supplier.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Salsa / Nachos Meal with Red Vegetable, Item # 61419

Product Codes/Lot Numbers:

Lot #'s: 1) 5322, 2) 6004, 3) 6039, 4) 6046, 5) 6057, 6) 6074, 7) 6090, 8) 6116, 9) 6124, 10) 6127, 11) 6130, 12) 6137, 13) 6146, 14) 6639, 15) 6646 Best Used By: 1) 5/21/16, 2) 7/8/16, 3) 7/17/16 & 9/16/16, 4) 9/22/16, 5) 9/2/16 & 9/22/16, 6) 10/28/16, 7) 12/1/16, 8) 12/1/16 & 12/16/16, 9) 12/1/16, 10) 10/30/16, 11) 12/1/16, 12) 12/1/16 & 12/14/16, 13) 9/22/16, 14) 7/17/16, 15) 9/22/16

Distribution:

Distributed in: CA, KS, KY, TN, TX, UT, VA, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0637-2017

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