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 Pecans 25 lbs., 15 lbs., 10 lbs., | Not published in this source record | 1,797 | Retail Dark Chocolate Pecans products manufactured between 01/14/16 to 10/24/17; and Bulk Dark Chocolate Pecans products manufactured between 01/14/16 to 09/05/2017. Lots: Lot# 479 Lot# 483 Lot# 505 Lot# 507 Lot# 05416 Lot# 13916 Lot# 16916 Lot# 25716 Lot# 30116 Lot# 31916 Lot# 06717 Lot# 13017 Lot# 23617 Lot# 23617B Lot# 07716 Lot# 10516 Lot# 30116 Lot# 31916 Lot# 04717 Lot# 08416 Lot# 10516 Lot# 10516 Lot# 15216 Lot# 16916 Lot# 19616 Lot# 22216 Lot# 25816 Lot# 26716 Lot# 31916 Lot# 35616 Lot# 35616 Lot# 04717 Lot# 06717 Lot# 13017 Lot# 16617 Lot# 21517 Lot# 23617 Lot# 24817B Lot# 02317 Lot# 27117 Lot# 20016 Lot# 30716 |
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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