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High RiskFDAfda-F-1877-2017CHOKING

Choklad Ljus Milk Chocolate Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.

Category
Units Affected
2,280,300
Recall Date
June 9, 2016
Issuing Agency
Hazard
Choking

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1877-2017.

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 LJUS Milk Chocolate Bar, 3.5 oz. (100g), UPC: 1402939250003; the manufacturing process adds the undeclared ingredients Hazelnut and Almond . The labeling carries a "May Contain" statement identifying almond and hazelnuts.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1877-2017.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Ikea North America Srvcs Inc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1877-2017.

Ikea North America Srvcs Inc

FDA

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Ikea North America Srvcs Inc Recall FAQ

Ikea North America Srvcs Inc is the subject of a dairy safety report: Choklad Ljus Milk Chocolate Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.. The notice was published on June 9, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 2,280,300 units are potentially affected.