EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and 80 items per case UPC 8 055880 00701 0 Manufactured by Bourbon 1-3-1 Ekimae Kashiwazaki Nigata 945-8611 Japan Product of Japan

Class I - Dangerous
Recalled: September 5, 2018 Wismettac Asian Foods (USA) Bakery & Bread Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot number not provided Item information: #64428A BISCUIT EVERY BURGER BOURBON (10/ 2.32 OZ) #64428B BISCUIT EVERY BURGER BOURBON (8/ 10/ 2.32 OZ)
  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:
Wismettac Asian Foods (USA) dba Nishimoto Trading Co Ltd
Reason for Recall:
The ingredient list and allergen information are partially covered by a nutrition sticker. Allergens of wheat, milk and eggs are visible.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and 80 items per case UPC 8 055880 00701 0 Manufactured by Bourbon 1-3-1 Ekimae Kashiwazaki Nigata 945-8611 Japan Product of Japan

Product Codes/Lot Numbers:

Lot number not provided Item information: #64428A BISCUIT EVERY BURGER BOURBON (10/ 2.32 OZ) #64428B BISCUIT EVERY BURGER BOURBON (8/ 10/ 2.32 OZ)

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0017-2019

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