Euro Custard Cake, Plastic wrapped cardboard container (Net Wt. 7.20 oz.)

Class I - Dangerous
Recalled: June 23, 2016 Eastland Food Bakery & Bread

What Should You Do?

  1. Check if you have this product:
    Item Code: 240304; Best Before 5/25/2017
  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:
Eastland Food Corporation
Reason for Recall:
The New York Department of Agriculture and Markets tested the Euro Custard Cake an detected that the product contained milk. The label did not declare milk and list it as an allergen on the label. Eastland Food Corporation became aware of these results on June 21 when FDA visited it facility. Eastland Food Corporation performed an investigation into the matter and determine late on June 22 that a single lot (310 cases) of product was missing this information. To this point no adverse incidents have been reported due to the mislabeling. Health risk assessment, people who have an allergy or severe sensitivity to milk run the risk of a serious or life threatening allergic reaction if they consume the affected Euro Custard Cakes under the mistaken assumption that it does not contain milk.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Euro Custard Cake, Plastic wrapped cardboard container (Net Wt. 7.20 oz.)

Product Codes/Lot Numbers:

Item Code: 240304; Best Before 5/25/2017

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2024-2016

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