🔍 RecallPedia

Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was MIS-LABELED as Angel Food Cake Bar. The label of Angel Food Cake Bar has the UPC 111110-02100. The label is read in parts: "***Angel Food Cake Bar *** Net wt. 12 oz *** Contains: Wheat and Eggs *** Distributed by Inter-American Products, Inc. Cincinnati, OH 45202***".

Class I - Dangerous
Recalled: October 14, 2018 Fred Meyer Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Time Stamp (HH/MM) followed by FK 285F
  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:
Fred Meyer Inc.
Reason for Recall:
Angel Food Cake Bar was recalled due to undeclared milk and soy. The actual product inside container is corn breads and it was mislabeled as Angel Food Cake Bar.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was MIS-LABELED as Angel Food Cake Bar. The label of Angel Food Cake Bar has the UPC 111110-02100. The label is read in parts: "***Angel Food Cake Bar *** Net wt. 12 oz *** Contains: Wheat and Eggs *** Distributed by Inter-American Products, Inc. Cincinnati, OH 45202***".

Product Codes/Lot Numbers:

Time Stamp (HH/MM) followed by FK 285F

Distribution:

Distributed in: OR, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0371-2019

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