Device recall
Z-2953-2024: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional…
FDA device recall · Class II · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Key facts
| Recall number (Z-number) | Z-2953-2024 |
|---|---|
| Recall event | 95148 |
| Product | Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Numbers 722079 and 722224 |
| Product code | OWB |
| Recalling firm | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K200917 |
| 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