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Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.

Class I - Dangerous
Recalled: June 9, 2016 Ikea North America Srvcs Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    All Best By dates
  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:
Ikea North America Srvcs Inc
Reason for Recall:
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD N¿T Milk Chocolate with Hazelnut, 3.5 oz. (100g), UPC: 120293926000: the manufacturing process adds the undeclared ingredient almond to the product. The labeling carries a "May Contain" statement identifying Almond.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.

Product Codes/Lot Numbers:

All Best By dates

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1878-2017

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