Wilderness Family Naturals Coconut Milk, Powdered, Organic packaged in the following sizes: 1) 16 oz foil pouch, UPC 98392-00769; 2) 12 lb. Case of 12 - 1 lbs packages, UPC 01002457 3) 5 lb. bag, UPC 98392-00770 4) 30 lb. Case of 6 - 5 lb. packages, UPC 01002458 5) Case of 1-55 lb. package, UPC 01002459 6) Trial Sample size, UPC 01002463

Class I - Dangerous
Recalled: February 12, 2016 Wilderness Family Naturals Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 1000011218, 1000012366, 1000013229. Best By Dates: 5/20/2017, 12/8/2017, 8/15/2018
  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:
Wilderness Family Naturals, LLC
Reason for Recall:
Wilderness Family Naturals Organic Coconut Milk Powder and other products that contain this as an ingredient are being recalled due to potential milk contamination.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Wilderness Family Naturals Coconut Milk, Powdered, Organic packaged in the following sizes: 1) 16 oz foil pouch, UPC 98392-00769; 2) 12 lb. Case of 12 - 1 lbs packages, UPC 01002457 3) 5 lb. bag, UPC 98392-00770 4) 30 lb. Case of 6 - 5 lb. packages, UPC 01002458 5) Case of 1-55 lb. package, UPC 01002459 6) Trial Sample size, UPC 01002463

Product Codes/Lot Numbers:

Lot Numbers: 1000011218, 1000012366, 1000013229. Best By Dates: 5/20/2017, 12/8/2017, 8/15/2018

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0757-2016

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