GKI Foods, LLC Recall: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.

🇺🇸 United States

1. October 27, 2017 - Recall initiated
2. November 29, 2017 - Reported by source
3. July 9, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0323-2018

Event ID

78405

Status

Terminated

Classification

Class II

Company

GKI Foods, LLC

Product description

Dark Chocolate Ginger , 25 lbs., 15 lbs.,

Quantity

6,699 cases

Reason

GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.

Recall initiation date

October 27, 2017

Report date

November 29, 2017

Classification date

Not published in this source record

Termination date

July 9, 2018

Distribution pattern

Domestic: MI, IN, IL, FL, TX, CA., NV, OR, NH, NY, NJ, VA, WI, KY, DE, PA, CT, PR, OH, RI, IA,

UPC, lot, and code information

All products manufactured between 01/14/16 to 10/24/17; Lots: Lot# 044 Lot# 044 Lot# 044 Lot# 047 Lot# 047 Lot# 047 Lot# 26217B Lot# 29217 Lot# 22216 Lot# 23716 Lot# 10917 Lot# 12917 Lot# 12917 Lot# 08416 Lot# 08416 Lot# 14016 Lot# 14016 Lot# 14616 Lot# 16116 Lot# 17416 Lot# 18816 Lot# 19516 Lot# 28716 Lot# 28816 Lot# 31516 Lot# 35516 Lot# 01917 Lot# 04017 Lot# 04017 Lot# 04017 Lot# 06517 Lot# 06717 Lot# 07517 Lot# 24817B Lot# 26217B Lot# 27717B Lot# 27717B Lot# 27717B Lot# 03516 Lot# 03516 Lot# 08416 Lot# 11916 Lot# 11916 Lot# 16116 Lot# 23716 Lot# 28416 Lot# 32816 Lot# 01917 Lot# 06117 Lot# 08717 Lot# 11117 Lot# 15617 Lot# 20717 Lot# 23417 Lot# 23417B Lot# 01917 Lot# 10717 Lot# 13917 Lot# 22217 Lot# 04616 Lot# 10416 Lot# 04017 Lot# 02516 Lot# 02516 Lot# 02516 Lot# 03516 Lot# 03516 Lot# 03516 Lot# 03516 Lot# 04616 Lot# 04616 Lot# 06016 Lot# 05716 Lot# 06016 Lot# 08416 Lot# 08416 Lot# 09716 Lot# 09716 Lot# 10416 Lot# 11216 Lot# 11216 Lot# 11216 Lot# 11216 Lot# 11216 Lot# 12416 Lot# 12416 Lot# 13316 Lot# 14016 Lot# 14016 Lot# 14616 Lot# 14016 Lot# 14616 Lot# 14616 Lot# 14016 Lot# 14616 Lot# 14616 Lot# 16116 Lot# 17416 Lot# 18816 Lot# 18816 Lot# 23716 Lot# 23716 Lot# 23716 Lot# 23716 Lot# 25016 Lot# 25016 Lot# 25016 Lot# 25016 Lot# 25016 Lot# 25016 Lot# 25816 Lot# 25816 Lot# 28716 Lot# 28516 Lot# 28516 Lot# 28716 Lot# 28816 Lot# 28816 Lot# 30516 Lot# 30516 Lot# 30516 Lot# 30516 Lot# 31516 Lot# 31516 Lot# 31516 Lot# 33516 Lot# 33516 Lot# 33516 Lot# 35516 Lot# 35516 Lot# 35516 Lot# 35516 Lot# 35516 Lot# 00517 Lot# 00517 Lot# 00517 Lot# 00517 Lot# 00517 Lot# 00517 Lot# 00517 Lot# 03217 Lot# 04017 Lot# 06117 Lot# 06117 Lot# 06017 Lot# 06717 Lot# 06717 Lot# 07517 Lot# 07517 Lot# 06717 Lot# 06717 Lot# 08717 Lot# 08117 Lot# 08717 Lot# 08717 Lot# 09417 Lot# 10317 Lot# 10717 Lot# 11117 Lot# 11117 Lot# 11117 Lot# 13917 Lot# 15617 Lot# 15617 Lot# 15617 Lot# 15617 Lot# 19517 Lot# 19517 Lot# 19517 Lot# 19517 Lot# 19517 Lot# 19517 Lot# 21317 Lot# 21317 Lot# 21317 Lot# 21317 Lot# 22217 Lot# 22217 Lot# 22817 Lot# 22217 Lot# 23417 Lot# 23417 Lot# 23417 Lot# 24817B Lot# 26217B Lot# 26217B Lot# 27717B Lot# 27717 Lot# 29217 Lot# 03317 Lot# 03317 Lot# 03217 Lot# 04017 Lot# 06016 Lot# 25816 Lot# 28516 Lot# 30516 Lot# 32616 Lot# 06517 Lot# 12417 Lot# 21317 Lot# 22817

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

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 78405 with 10 other product entries in Public Health Trace.

Responsible company: GKI Foods, LLC

Other recalls from GKI Foods, LLC

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
Michigan	1
Indiana	1
Illinois	1
Florida	1
Texas	1
California	1
Nevada	1
Oregon	1
New Hampshire	1
New York	1
New Jersey	1
Virginia	1
Wisconsin	1
Kentucky	1
Delaware	1
Pennsylvania	1
Connecticut	1
Puerto Rico	1
Ohio	1
Rhode Island	1
Iowa	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.

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