Thunder Jack Cheese sold under the following brand names: Amish Classic Firecracker & Guggisberg
Recalling firm: Guggisberg Cheese Inc
Why it was recalled
The firm was notified that the product may contain Listeria monocytogenes.
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ProductThunder Jack Cheese sold under the following brand names: Amish Classic Firecracker & Guggisberg
FDA code information
Item # 63062, Lot # 0916167, 0930162, 1014167 & 1028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166.
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Full FDA record and distribution details
Original product description
Thunder Jack Cheese sold under the following brand names: Amish Classic Firecracker & Guggisberg
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 0902164 | 028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 09021 |
| lot | 0902164 | m # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166. |
| lot | 0902165 | tem # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 09301 |
| lot | 0902166 | # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166. |
| lot | 0902167 | 5, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166. |
| lot | 0916166 | 604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 09301 |
| lot | 0916167 | Item # 63062, Lot # 0916167, 0930162, 1014167 & 1028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, |
| lot | 0916167 | Item # 63062, Lot # 0916167, 0930162, 1014167 & 1028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 09021 |
| lot | 0916167 | 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166. |
| lot | 0930162 | Item # 63062, Lot # 0916167, 0930162, 1014167 & 1028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & |
| lot | 0930164 | -70, Lot # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166. |
| lot | 0930168 | # 0902166, 0902167, 0916167 & 0930168; Item # D0602-71, Lot # 0902164, 0930164, 0930168 & 1014166. |
| lot | 1014167 | Item # 63062, Lot # 0916167, 0930162, 1014167 & 1028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 091616 |
| lot | 1014167 | 63062, Lot # 0916167, 0930162, 1014167 & 1028167; Item # 630604, Lot # 0916167, 1014167 & 1028167; Item # D0602-65, Lot # 0902164, 0902165, 0916166 & , 0916167; Item # D0602-70, Lot # 0902166, 0902167, 09161 |
Recall details
- Recall number
- F-2107-2017
- Event ID
- 76469
- FDA status
- Terminated
- Initiated
- Feb 14, 2017
- Reported
- May 3, 2017
- Classified
- Apr 21, 2017
- Terminated
- Feb 22, 2018
- Quantity
- 2,051 cases
- Location
- Millersburg, OH, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Product was shipped to the following states: AL, AZ, GA, IL, IN, KY, MD, MI, NV, OH, PA, WI & WV.
FDA source record · F-2107-2017
Data updated September 16, 2026. View official FDA data ↗
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