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-0314-2018

Event ID

78405

Status

Terminated

Classification

Class II

Company

GKI Foods, LLC

Product description

Dark Chocolate Banana Chips, 25 lbs., 8/8 oz., 8 pc. display,

Quantity

2,287 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# 34316 Lot# 01817 Lot# 11/28/2016P1 Lot# 11/28/2016P1 Lot# 12/04/2016P1 Lot# 01/23/2017P1 Lot# 03/06/2017P1 Lot# 04/16/2017P1 Lot# 05/14/2017P1 Lot# 07/24/2017P1 Lot# 10/31/2017P1 Lot# 06/25/2018P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1 Lot# 12517 Lot# 24817 Lot# 01816 Lot# 01816 Lot# 06316 Lot# 08216 Lot# 14016 Lot# 16516 Lot# 18916 Lot# 23616 Lot# 29516 Lot# 29516 Lot# 34316 Lot# 05317 Lot# 09317 Lot# 12517 Lot# 14417 Lot# 24117 Lot# 08216 Lot# 12316 Lot# 16516 Lot# 20116 Lot# 28416 Lot# 28416 Lot# 34316 Lot# 09317 Lot# 11117 Lot# 12517 Lot# 04816 Lot# 04816 Lot# 06316 Lot# 06316 Lot# 10016 Lot# 10016 Lot# 12316 Lot# 12316B Lot# 12716B Lot# 12716B Lot# 12716 Lot# 12716 Lot# 14016 Lot# 15416 Lot# 16516 Lot# 20116 Lot# 23616 Lot# 31716 Lot# 32116 Lot# 07217 Lot# 09317 Lot# 10817 Lot# 12517 Lot# 14417 Lot# 18017 Lot# 24117 Lot# 27817 Lot# 27817 Lot# 04116 Lot# 04816 Lot# 06316 Lot# 12716B Lot# 26316 Lot# 00517 Lot# 01817 Lot# 11117 Lot# 24817 Lot# 20816 Lot# 20116 Lot# 20816 Lot# 26816 Lot# 29516 Lot# 11117 Lot# 12517 Lot# 13917 Lot# 18017 Lot# 18017 Lot# 24817 Lot# 06016 Lot# 14016 Lot# 28016 Lot# 32116 Lot# 04017 Lot# 14417 Lot# 23417 Lot# 04116 Lot# 10016 Lot# 15416 Lot# 20816 Lot# 05517 Lot# 11117 Lot# 14417 Lot# 22217 Lot# 17516 Lot# 20816 Lot# 28416 Lot# 09017 Lot# 18017+F98F89:F128F81:F128D17FF4:F128

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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