Z-2441-2019 Class II Terminated
FDA device recall Z-2441-2019 was initiated by Fujifilm Medical Systems U.S.A., Inc. on July 19, 2019 and is designated Class II. Reason for recall: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD) The recall status is terminated (terminated August 28, 2020). Affected quantity: 174 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 11, 2019
- Initiation Date
- July 19, 2019
- Termination Date
- August 28, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 174 units
Product Description
Fujifilm FDR Go Plus mobile X-ray system
Reason for Recall
The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
Distribution Pattern
Nationwide
Code Information
All serial numbers