Device recall
Z-0907-2022: Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614…
FDA device recall · Class I · Respironics California, LLC
Key facts
| Recall number (Z-number) | Z-0907-2022 |
|---|---|
| Recall event | 89767 |
| Product | Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618, 1076709, 1076716, 1076717, 1137292, DU1053617, U1053617, R1053618, R1076709) |
| Product code | MNT |
| Recalling firm | Respironics California, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K102985 |
| FEI number | 2518422 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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