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 Coconut Bites, 25 lbs., 12/10 oz. | Not published in this source record | 979 cases | All products manufactured between 01/14/16 to 10/24/17; Lots: Lot# 06416 Lot# 27316 Lot# 27316 Lot# 30316 Lot# 34016 Lot# 34016 Lot# 06017 Lot# 11717B Lot# 11717 Lot# 21217 Lot# 23617 Lot# 07217 Lot# 10817 Lot# 11417 Lot# 11417B Lot# 16717 Lot# 23617 Lot# 27316 Lot# 12/07/2016P1 Lot# 01/10/2017P1 Lot# 02/20/2017P1 Lot# 05/02/2017P1 Lot# 08/06/2017P1 Lot# 12/27/2017P1 Lot# 01/02/2018P1 Lot# 03/28/2018P1 Lot# 04/01/2018P1 Lot# 04/15/2018P1 Lot# 04/22/2018P1 Lot# 04/23/2018P1 |
This recall shares FDA event ID 78405 with 10 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
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.
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