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-0316-2018

Event ID

78405

Status

Terminated

Classification

Class II

Company

GKI Foods, LLC

Product description

Dark Chocolate Almond Bark 10 oz.,10 lbs.

Quantity

1,517 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# 01916B Lot# 04216 Lot# 08916 Lot# 10216 Lot# 13216B Lot# 16016B Lot# 19316B Lot# 19416B Lot# 22316 Lot# 26016 Lot# 26316 Lot# 30516 Lot# 30616 Lot# 30616 Lot# 27516B Lot# 31416 Lot# 32016 Lot# 35416B Lot# 35516 Lot# 10817B Lot# 11617 Lot# 11617 Lot# 12917 Lot# 15917 Lot# 17117 Lot# 19317 Lot# 19417 Lot# 21917B Lot# 23417 Lot# 27617B Lot# 27917 Lot# 04216 Lot# 08216B Lot# 08216B Lot# 10216 Lot# 10216B Lot# 13216B Lot# 13816 Lot# 20916 Lot# 20916 Lot# 22316 Lot# 22316 Lot# 25616B Lot# 25816 Lot# 25816B Lot# 25916 Lot# 25916B Lot# 26016 Lot# 27516B Lot# 30616 Lot# 33516 Lot# 34916 Lot# 35016 Lot# 01817 Lot# 02317 Lot# 04617 Lot# 19417 Lot# 19417 Lot# 19517 Lot# 19817 Lot# 19917 Lot# 20117 Lot# 20517 Lot# 08216B Lot# 08916 Lot# 00616B Lot# 01916B Lot# 06016 Lot# 08216B Lot# 10216B Lot# 10216B Lot# 13216B Lot# 13816 Lot# 13816 Lot# 16016B Lot# 18016 Lot# 18116 Lot# 20016 Lot# 20716B Lot# 20916 Lot# 23516 Lot# 23916 Lot# 27516B Lot# 32016 Lot# 33516 Lot# 33516 Lot# 34916 Lot# 35016 Lot# 35516 Lot# 35516B Lot# 05517 Lot# 05917B Lot# 06217 Lot# 06517 Lot# 06517 Lot# 09417 Lot# 09417 Lot# 10817B Lot# 12917 Lot# 15917 Lot# 18617 Lot# 19317 Lot# 20517 Lot# 21217B Lot# 21917B Lot# 23417 Lot# 24817 Lot# 25117 Lot# 26517B Lot# 04216 Lot# 05616 Lot# 06016 Lot# 19416B Lot# 19516 Lot# 20016 Lot# 22316B Lot# 23316 Lot# 23516 Lot# 26416B Lot# 27516B Lot# 34916 Lot# 35016 Lot# 01317 Lot# 01817 Lot# 02317 Lot# 05517 Lot# 09417 Lot# 17117 Lot# 18617 Lot# 26517B Lot# 27917 Lot# 29217 Lot# 26316 Lot# 24817 Lot# 25017

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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