FDA Device recall Z-2441-2019
Fujifilm FDR Go Plus mobile X-ray system
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of Fujifilm FDR Go Plus mobile X-ray system by Fujifilm Medical Systems U, citing the graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2441-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-19 |
| Published | 2019-09-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Fujifilm Medical Systems U |
| Distribution | US |
Product
Fujifilm FDR Go Plus mobile X-ray system
Reason
The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
Identifiers
| code_info | All serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2441-2019%22
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