Dark Chocolate Powerberry, 12/8 oz., 25 lbs.
Recalling firm: GKI Foods, LLC
Why it was recalled
GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.
The exact product
Dark Chocolate Powerberry, 12/8 oz., 25 lbs.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
All products manufactured between 01/14/16 to 10/24/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1
| Type | Code / value | Context |
|---|---|---|
| lot | 03/13/2018P1 | 6917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
| lot | 03/19/2018P1 | ot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
| lot | 048 | All products manufactured between 01/14/16 to 10/24/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/ |
| lot | 049 | All products manufactured between 01/14/16 to 10/24/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 |
| lot | 10/15/2017P1 | en 01/14/16 to 10/24/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
| lot | 10/15/2017P1 | 4/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
| lot | 10/15/2017P1 | ot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
| lot | 10/16/2017P1 | 8 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
| lot | 26917 | ducts manufactured between 01/14/16 to 10/24/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/ |
| lot | 29417 | ctured between 01/14/16 to 10/24/17, Lots: Lot# 048 Lot# 049 Lot# 26917 Lot# 29417 Lot# 10/15/2017P1 Lot# 10/15/2017P1 Lot# 10/16/2017P1 Lot# 03/13/2018P1 Lot# 03/19/2018P1 Lot# 10/15/2017P1 |
Recall details
- Recall number
- F-0327-2018
- Event ID
- 78405
- FDA status
- Terminated
- Initiated
- Oct 27, 2017
- Reported
- Nov 29, 2017
- Classified
- Nov 17, 2017
- Terminated
- Jul 9, 2018
- Quantity
- 628 cases
- Location
- Brighton, MI, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
Domestic: MI, IN, IL, FL, TX, CA., NV, OR, NH, NY, NJ, VA, WI, KY, DE, PA, CT, PR, OH, RI, IA,
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.