Check the Batch
Class IITerminated in FDA datasetRecall initiated Oct 27, 2017

Dark Chocolate Pineapple, 8/ 8oz., 8 pc/display

Recalling firm: GKI Foods, LLC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 9, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductDark Chocolate Pineapple, 8/ 8oz., 8 pc/display
Package size8oz

FDA code information

All products manufactured between 01/14/16 to 10/24/17; Lot# 11/28/2016P1 Lot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Dark Chocolate Pineapple, 8/ 8oz., 8 pc/display

Extracted codes and context

TypeCode / valueContext
lot01/16/2017P1All products manufactured between 01/14/16 to 10/24/17; Lot# 11/28/2016P1 Lot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot#
lot02/21/2018P1ot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1
lot02/21/2018P1ot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1
lot02/21/2018P1ot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1
lot04/12/2017P1ctured between 01/14/16 to 10/24/17; Lot# 11/28/2016P1 Lot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot#
lot05/17/2017P14/16 to 10/24/17; Lot# 11/28/2016P1 Lot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot#
lot05/27/2018P1ot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1
lot07/24/2017P1ot# 11/28/2016P1 Lot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot#
lot07/25/2017P1ot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot#
lot11/01/2017P1ot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot#
lot11/16/2017P1ot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1
lot11/16/2017P1ot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1
lot11/28/2016P1All products manufactured between 01/14/16 to 10/24/17; Lot# 11/28/2016P1 Lot# 01/16/2017P1 Lot# 04/12/2017P1 Lot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot#
lot11/28/2016P1ot# 05/17/2017P1 Lot# 07/24/2017P1 Lot# 07/25/2017P1 Lot# 11/01/2017P1 Lot# 11/28/2016P1 Lot# 11/16/2017P1 Lot# 11/16/2017P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 02/21/2018P1 Lot# 05/27/2018P1

Original FDA recall reason

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

Recall details

Recall number
F-0326-2018
Event ID
78405
FDA status
Terminated
Initiated
Oct 27, 2017
Reported
Nov 29, 2017
Classified
Nov 17, 2017
Terminated
Jul 9, 2018
Quantity
987 cases
Location
Brighton, MI, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

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

FDA source record · F-0326-2018

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.