Ezekiel 4:9 Sprouted Grain Cereal- Golden Flax, 16 oz. Packaging label reads in part:" Food FOR Life***EZEKIEL 4:9 SPROUTED WHOLE GRAIN CEREAL GOLDEN FLAX***NET WT. 16 OZ(454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434***".

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UPC 07347200256 8 LOT numbers: M3253, M3309, M3414, M3439, M3523, N0068, N0165 Best by dates: NOV. 24, 2013 DEC. 5, 2013 DEC. 11, 2013 DEC. 18, 2013 DEC. 21, 2013 JAN. 14, 2014 JAN. 15, 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:
Food For Life Baking Company Inc.
Reason for Recall:
The firm is recalling Ezekiel 4:9 Sprouted Grain Cereal because the product may be mislabeled and may contain an undeclared allergen - almond.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Ezekiel 4:9 Sprouted Grain Cereal- Golden Flax, 16 oz. Packaging label reads in part:" Food FOR Life***EZEKIEL 4:9 SPROUTED WHOLE GRAIN CEREAL GOLDEN FLAX***NET WT. 16 OZ(454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434***".

Product Codes/Lot Numbers:

UPC 07347200256 8 LOT numbers: M3253, M3309, M3414, M3439, M3523, N0068, N0165 Best by dates: NOV. 24, 2013 DEC. 5, 2013 DEC. 11, 2013 DEC. 18, 2013 DEC. 21, 2013 JAN. 14, 2014 JAN. 15, 2014

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1142-2013

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