Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT 4 LB 8 OZ, KEEP FROZEN, UPC 0 49800 04776 1 (retail), Product Code 04776 --- Rich Products Corp., Buffalo, NY 14213

Class I - Dangerous
Recalled: December 21, 2016 Rich Products Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    Retail: Best By JUN-27-17, JUL-15-17, JUL-23-17, JUL-28-17, AUG-27-17 (Best By date code found on side of each individual unit package); -- Product Code 04776: Julian Dates 14076274, 14076292, 14076300, 14076305, 14076335.
  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:
Rich Products Corp
Reason for Recall:
The product may contain undeclared walnuts from intermediate layer cake supplier.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT 4 LB 8 OZ, KEEP FROZEN, UPC 0 49800 04776 1 (retail), Product Code 04776 --- Rich Products Corp., Buffalo, NY 14213

Product Codes/Lot Numbers:

Retail: Best By JUN-27-17, JUL-15-17, JUL-23-17, JUL-28-17, AUG-27-17 (Best By date code found on side of each individual unit package); -- Product Code 04776: Julian Dates 14076274, 14076292, 14076300, 14076305, 14076335.

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1363-2017

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