Drug recall
Fujifilm FDR Go Plus mobile X-ray system
FDA recall event 83524 · Class II · Fujifilm Medical Systems U.S.A., Inc.
Key facts
| Event ID | 83524 |
|---|---|
| Recall numbers | Z-2441-2019 |
| Recalling firm | Fujifilm Medical Systems U.S.A., Inc. |
| Product type | Devices |
| Products | Fujifilm FDR Go Plus mobile X-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD) |
| Initiation date | Jul 19, 2019 |
| Report date | Sep 11, 2019 |
| Termination date | Aug 28, 2020 |
| City | Lexington |
| State | MA |
| Country | United States |
| FEI number | 1000513161 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: