Device recall
Z-0612-2019: Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary…
FDA device recall · Class II · Philips Medical Systems Gmbh, DMC
Key facts
| Recall number (Z-number) | Z-0612-2019 |
|---|---|
| Recall event | 81706 |
| Product | Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System |
| Product code | JAA |
| Recalling firm | Philips Medical Systems Gmbh, DMC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2020 |
| 510(k) numbers | K163210 |
| FEI number | 3003768251 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database