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 Ginger Snap Cookies, 10 lbs. | Not published in this source record | 613 Cases | All products manufactured between 01/14/16 to 10/24/17; Lots: Lot# 04116 Lot# 04116 Lot# 07016 Lot# 07016 Lot# 08116 Lot# 07016 Lot# 08916 Lot# 08916 Lot# 10416 Lot# 10416 Lot# 11116B Lot# 11116B Lot# 13016 Lot# 15216 Lot# 15216 Lot# 18016 Lot# 18016 Lot# 18016 Lot# 20716 Lot# 23016B Lot# 23016B Lot# 25016 Lot# 25016 Lot# 27916 Lot# 28416 Lot# 28416 Lot# 28416B Lot# 28416B Lot# 30216 Lot# 30216 Lot# 32616B Lot# 33716B Lot# 32616B Lot# 33716B Lot# 01617 Lot# 01717 Lot# 01717 Lot# 01717 Lot# 06617B Lot# 06617B Lot# 08817B Lot# 08817B Lot# 18617 Lot# 18617 Lot# 18617 Lot# 21917 Lot# 20716 |
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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