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-0332-2018

Event ID

78405

Status

Terminated

Classification

Class II

Company

GKI Foods, LLC

Product description

Dark Chocolate Turbinado Sea Salt Almonds , 15 lbs., 10 lbs., 18/14 oz.,

Quantity

12,097 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 Turbinado Sea Salt Almonds manufactured between 01/14/16 to 10/24/17; and Bulk Dark Chocolate Turbinado Sea Salt Almonds; Lot numbers: LOT# Lot# 068 Lot# 074 Lot# 02816 Lot# 04916 Lot# 07416 Lot# 11616B Lot# 11616 Lot# 11816 Lot# 11816B Lot# 12416B Lot# 12416 Lot# 13816 Lot# 13816B Lot# 14416B Lot# 16016 Lot# 21716 Lot# 22216 Lot# 26316B Lot# 28516 Lot# 29116 Lot# 29216 Lot# 00317 Lot# 01317 Lot# 03217 Lot# 03217B Lot# 09417 Lot# 10117 Lot# 10117B Lot# 12217B Lot# 12217 Lot# 14417 Lot# 15917 Lot# 15917B Lot# 20517B Lot# 25517B Lot# 25817B Lot# 26317B Lot# 26317 Lot# 25616B Lot# 160 Lot# 162 Lot# 134 Lot# 136 Lot# 137 Lot# 21716 Lot# 25616B Lot# 170 Lot# 171 Lot# 175 Lot# 176 Lot# 18817 Lot# 18817B Lot# 22217 Lot# 22217 Lot# 25517B Lot# 25517 Lot# 25817B Lot# 26917 Lot# 26917B Lot# 27117B Lot# 27117 Lot# 113 Lot# 134 Lot# 135 Lot# 136 Lot# 137 Lot# 138 Lot# 03916 Lot# 06216 Lot# 11616B Lot# 16016 Lot# 21716 Lot# 02/19/2017T Lot# 04/02/2017T Lot# 05/02/2017T Lot# 06/04/2017T Lot# 06/04/2017T Lot# 07/31/2017T Lot# 09/24/2017T Lot# 10/02/2017T Lot# 12/06/2017T Lot# 01/15/2018T Lot# 12/06/2017T Lot# 01/15/2018T Lot# 03/27/2018T Lot# 04/22/2018T Lot# 06/06/2018T Lot# 03/31/2019T Lot# 433 Lot# 436 Lot# 442 Lot# 22217 Lot# 25817B Lot# 28517 Lot# 11816 Lot# 08817 Lot# 11816 Lot# 20416 Lot# 27516B Lot# 06617 Lot# 12217B Lot# 24117B Lot# 04916 Lot# 09716 Lot# 09716 Lot# 14416B Lot# 26316B Lot# 32316 Lot# 01317 Lot# 05517 Lot# 06617 Lot# 10117 Lot# 14617 Lot# 02816 Lot# 02816 Lot# 02816 manufactured between 01/14/16 to 09/05/2017

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.

• Email
• X / Twitter
• Facebook