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 Pretzel Balls, 15 lbs. | Not published in this source record | N/A | Retail Dark Chocolate Pretzel Balls manufactured between 01/14/16 to 10/24/17; and Bulk Dark Chocolate Pretzel Balls manufactured between 01/14/16 to 09/05/2017; Lots: Lot# 08316 Lot# 20116B Lot# 27316B Lot# 27316 Lot# 06017 Lot# 22717 Lot# 27717 Lot# 03916 Lot# 08316 Lot# 08316 Lot# 14416 Lot# 14416 Lot# 18816 Lot# 19416 Lot# 21416 Lot# 23616 Lot# 32716 Lot# 34916 Lot# 06017 Lot# 07317 Lot# 08117 Lot# 09317 Lot# 10217 Lot# 19917 Lot# 21217 Lot# 24817 Lot# 27416 |
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.
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