Device recall
Z-0899-2021: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage…
FDA device recall · Class II · Respironics California, LLC
Key facts
| Recall number (Z-number) | Z-0899-2021 |
|---|---|
| Recall event | 86646 |
| Product | Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories. |
| Product code | MNT |
| Recalling firm | Respironics California, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2024 |
| 510(k) numbers | K082660 |
| FEI number | 2518422 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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