Ikea North America Srvcs Inc 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 MORK Dark Chocolate Bar, 3.5 oz. (100g), UPC: 1002939270003. Product has a may contain qualifying statement for milk, Almond and Hazelnut. The manufacturer's process adds Milk, Almond, Hazelnut to the chocolate but the label fails to declare milk, almond and hazelnut as ingredients. CHOKLAD MORK 70% Dark Chocolate Bars, 3.5 0z. (100g), UPC: 1203080940009, Contains: Milk, Almond, Hazelnut as ingredients. However, these allergens are declared in a "may contain statement" identifying the allergens as Milk and Treenuts.

🇺🇸 United States

1. June 9, 2016 - Recall initiated
2. April 12, 2017 - Reported by source
3. January 19, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1873-2017

Event ID

74526

Status

Terminated

Classification

Class II

Company

Ikea North America Srvcs Inc

Product description

Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ. Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.

Quantity

2,419,228 bars

Reason

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 MORK Dark Chocolate Bar, 3.5 oz. (100g), UPC: 1002939270003. Product has a may contain qualifying statement for milk, Almond and Hazelnut. The manufacturer's process adds Milk, Almond, Hazelnut to the chocolate but the label fails to declare milk, almond and hazelnut as ingredients. CHOKLAD MORK 70% Dark Chocolate Bars, 3.5 0z. (100g), UPC: 1203080940009, Contains: Milk, Almond, Hazelnut as ingredients. However, these allergens are declared in a "may contain statement" identifying the allergens as Milk and Treenuts.

Recall initiation date

June 9, 2016

Report date

April 12, 2017

Classification date

Not published in this source record

Termination date

January 19, 2018

Distribution pattern

AZ CA Co CT FL GA IL KS MA MD MI MN MO NC NJ NV NY OH OR PA TX UT VA WA

UPC, lot, and code information

All Best By dates

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Other

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 74526 with 5 other product entries in Public Health Trace.

Responsible company: Ikea North America Srvcs Inc

Other recalls from Ikea North America Srvcs Inc

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Arizona	1
California	1
Connecticut	1
Florida	1
Georgia	1
Illinois	1
Kansas	1
Massachusetts	1
Maryland	1
Michigan	1
Minnesota	1
Missouri	1
North Carolina	1
New Jersey	1
Nevada	1
New York	1
Ohio	1
Oregon	1
Pennsylvania	1
Texas	1
Utah	1
Virginia	1
Washington	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

• Email
• X / Twitter
• Facebook