Device recall
Z-1141-2019: Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002…
FDA device recall · Class II · Philips Medical Systems Nederlands
Key facts
| Recall number (Z-number) | Z-1141-2019 |
|---|---|
| Recall event | 82459 |
| Product | Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002 Allura Xper FD10 F 722003 Allura Xper FD10 722005 Allura Xper FD10/10 722006 Allura Xper FD20 722008 Allura Xper FD20 Biplane 722010 Allura Xper FD10 722011 Allura Xper FD10/10 722012 Allura Xper FD20 722013 Allura XPER… |
| Product code | IZI |
| Recalling firm | Philips Medical Systems Nederlands |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 14, 2020 |
| 510(k) numbers | K031333, K033737, K041949 |
| FEI number | 3002807880 |
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