Recall · FDA
GE Healthcare, LLC
GE Healthcare, LLC issued a Class II FDA recall (Z-0916-2017) initiated 2016-11-21: SFX
| Company | GE Healthcare, LLC |
|---|---|
| Recall number | Z-0916-2017 |
| Classification | Class II |
| Status | Terminated |
| Category | Devices |
| Initiated | 2016-11-21 |
| Product | SFX |
| Reason | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems. |
FAQ
What did GE Healthcare, LLC recall?
SFX
Why was GE Healthcare, LLC's product recalled?
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.