FDA Recall United States Terminated Historical recordClass II
GKI Foods, LLC
- Product
- Dark Chocolate Pretzel Nibs, 15 lbs.
- Published
- November 29, 2017
- Distribution
- Domestic: MI, IN, IL, FL, TX, CA., NV, O…
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Dark Chocolate Strawberries, 25 lbs., 8/7 oz., 8 pc. display, 10 lbs., | Not published in this source record | 4,418 cases | All products manufactured between 01/14/16 to 10/24/17; LOts: Lot# 02317 Lot# 09717 Lot# 11617B Lot# 14317 Lot# 29217B Lot# 11/23/201 Lot# 11/23/2016P1 Lot# 12/04/201P1 Lot# 01/23/201 Lot# 02/28/201 Lot# 03/01/201 Lot# 04/17/201 Lot# 05/17/201 Lot# 07/25/2017P1 Lot# 10/17/201 Lot# 11/01/201 Lot# 02/21/201 Lot# 06/11/201 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# 04517 Lot# 19817 Lot# 22316 Lot# 25216 Lot# 27216B Lot# 35116 Lot# 03117 Lot# 04517 Lot# 16517 Lot# 19417 Lot# 22717B Lot# 24317 Lot# 25117 Lot# 26417 Lot# 03516 Lot# 12616 Lot# 16116 Lot# 07716 Lot# 08916 Lot# 11716B Lot# 12016 Lot# 13916 Lot# 16116 Lot# 17316 Lot# 19016 Lot# 20316 Lot# 22316 Lot# 25216 Lot# 25216 Lot# 25216 Lot# 27216B Lot# 30916 Lot# 33716 Lot# 33716 Lot# 00617 Lot# 06717 Lot# 06717 Lot# 08717 Lot# 09717 Lot# 10717 Lot# 13717 Lot# 15117 Lot# 16517 Lot# 19417 Lot# 21517 Lot# 21517 Lot# 25117 Lot# 25117 Lot# 27117 Lot# 03416 Lot# 07716 Lot# 11716B Lot# 12616 Lot# 13916 Lot# 16216 Lot# 16216 Lot# 19016 Lot# 20316 Lot# 25216 Lot# 26716 Lot# 26716B Lot# 30216 Lot#30916 Lot# 32316 Lot# 33716 Lot# 35116 Lot# 04517 Lot# 05917 Lot# 07517 Lot# 08717 Lot# 13717 Lot# 14317 Lot# 16517 Lot# 19417 Lot# 19817 Lot# 22717B Lot# 22717 Lot# 26417 Lot# 27117 Lot# 07716 Lot# 08916 Lot# 10416 Lot# 11716B Lot# 12016 Lot# 12616 Lot# 15316 Lot# 17316 Lot# 18116 Lot# 19016 Lot# 23916 Lot# 24416 Lot# 25216 Lot# 26716 Lot# 28816 Lot# 30916 Lot# 30916 Lot# 32316 Lot# 35116 Lot# 35816 Lot# 00617 Lot# 03117 Lot# 04517 Lot# 05917 Lot# 06717 Lot# 09717 Lot# 13717 Lot# 16517 Lot# 18717 Lot# 19817 Lot# 21517 Lot# 24317 Lot# 25117 Lot# 27117 Lot# 04517 Lot# 05917 Lot# 13717 Lot# 19817 Lot# 26417 Lot# 11716 Lot# 12016 Lot# 12616 Lot# 13916 Lot# 15316 Lot# 16216 Lot# 18116 Lot #20316 Lot# 20316 Lot# 22316 Lot# 22316 Lot# 24416 Lot# 25216 Lot# 26716 Lot# 28816 Lot# 30216 Lot# 30916 Lot# 30916 Lot# 32316 Lot# 33716 Lot# 35116 Lot# 35816 Lot# 03117 Lot# 03117 Lot# 05917 Lot# 06717 Lot# 07517 Lot# 09717 Lot# 10717 Lot# 13717 Lot# 15117 Lot# 15117 Lot# 16517 Lot# 18717 Lot# 19417 Lot# 21517 Lot# 22717B Lot# 25117 Lot# 25117 Lot# 27117 Lot# 29217B |
This recall shares FDA event ID 78405 with 9 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
Responsible company: GKI Foods, LLC
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| 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.
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
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.
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.
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.
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