NACHO CHEESE TORTILLA CHIPS: Essential Everyday 1 oz bag (Multi-pak) UPC 4 13030 05979; Essential Everyday 1 oz bag UPC 4 13030 59821, 10 oz bag UPC 4 13030 37638 & Market Essential 11.5 oz bag UPC 9 84873 00119
Class I - DangerousWhat Should You Do?
- Check if you have this product: Essential Everyday 1 oz bag (Multi-pak) Best By 11/12/2016 - 4/01/2017 Essential Everyday 1 oz bag Best By 11/12/2016 - 3/10/2017 10 oz bag Best By 11/7/2016 - 3/31/2017 Market Essential 11.5 oz bag Best By 11/15/2016 -0 2/19/2017
- 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:
- Shearers Foods, Llc
- Reason for Recall:
- The firm is recalling various snack products because they used ingredients received from Valley Milk Product which may be contaminated with Salmonella
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
NACHO CHEESE TORTILLA CHIPS: Essential Everyday 1 oz bag (Multi-pak) UPC 4 13030 05979; Essential Everyday 1 oz bag UPC 4 13030 59821, 10 oz bag UPC 4 13030 37638 & Market Essential 11.5 oz bag UPC 9 84873 00119
Product Codes/Lot Numbers:
Essential Everyday 1 oz bag (Multi-pak) Best By 11/12/2016 - 4/01/2017 Essential Everyday 1 oz bag Best By 11/12/2016 - 3/10/2017 10 oz bag Best By 11/7/2016 - 3/31/2017 Market Essential 11.5 oz bag Best By 11/15/2016 -0 2/19/2017
Distribution:
Distributed in: AL, AZ, IA, IL, KS, MN, NE, OH, SD, TX, WI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1552-2017
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