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-0324-2018

Event ID

78405

Status

Terminated

Classification

Class II

Company

GKI Foods, LLC

Product description

Dark Chocolate Peanuts, 5 lbs.,15 lbs., 10 lbs., 25 lbs.

Quantity

8,541 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

Retail Dark Chocolate Peanuts manufactured between 01/14/16 to 10/24/17; and Bulk Dark Chocolate Peanuts manufactured between 01/14/16 to 09/05/2017; Lots: Lot# 02916 Lot# 12516 Lot# 22316 Lot# 30716 Lot# 05517 Lot# 13617 Lot# 24817B Lot# 11816 Lot# 17316 Lot# 18116 Lot# 25316 Lot# 27916 Lot# 00417 Lot# 04717 Lot# 12917 Lot# 17117 Lot# 22717 Lot# 26417B Lot# 01516 Lot# 01516 Lot# 02916 Lot# 04216 Lot# 04216 Lot# 06016 Lot# 08816 Lot# 08816B Lot# 11016B Lot# 11016B Lot# 12516 Lot# 13716 Lot# 14616B Lot# 16016 Lot# 16616 Lot# 18116 Lot# 19116 Lot# 19116 Lot# 23216 Lot# 23516 Lot# 25316 Lot# 27116 Lot# 30116 Lot# 31316 Lot# 31716 Lot# 34716 Lot# 01617 Lot# 04717 Lot# 07317 Lot# 09417 Lot# 11117 Lot# 12917 Lot# 12917 Lot# 15917 Lot# 15917 Lot# 17117 Lot# 17117 Lot# 19517 Lot# 19517 Lot# 20917 Lot# 22717 Lot# 24817B Lot# 24817B Lot# 24817B Lot# 27617 Lot# 31316 Lot# 04216 Lot# 07416 Lot# 08316 Lot# 08816B Lot# 08816 Lot# 08816B Lot# 11016B Lot# 11016 Lot# 11816 Lot# 14016 Lot# 14016 Lot# 15316 Lot# 15916 Lot# 16516 Lot# 16016 Lot# 17316 Lot# 16616 Lot# 17316 Lot# 25616 Lot# 25616B Lot# 25616B Lot# 25616 Lot# 27116 Lot# 27116B Lot# 28416B Lot# 28416B Lot# 28416 Lot# 30116 Lot# 33316 Lot# 35616 Lot# 00417 Lot# 01317 Lot# 05817 Lot# 07917 Lot# 09417 Lot# 11117 Lot# 12317 Lot# 14217 Lot# 19517 Lot# 19517 Lot# 21517 Lot# 24817B Lot# 26417 Lot# 28217 Lot# 23216 Lot# 24817B Lot# 14616B Lot# 14616 Lot# 01017 Lot# 05517 Lot# 06016 Lot# 19116 Lot# 22316 Lot# 29316 Lot# 28416B Lot# 11117 Lot# 12917 Lot# 19517 Lot# 32716 Lot# 02717 Lot# 11117 Lot# 02916 Lot# 19016 Lot# 25616B Lot# 31716 Lot# 05817 Lot# 08816B Lot# 05817 Lot# 13617 Lot# 08316 Lot# 14016 Lot# 19116 Lot# 28116 Lot# 01717 Lot# 18017 Lot# 28217 Lot# 27916 Lot# 04216 Lot# 07716 Lot# 10516 Lot# 14016 Lot# 29316 Lot# 04717

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 9 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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