Device recall
Z-2073-2021: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The…
FDA device recall · Class I · Respironics California, LLC
Key facts
| Recall number (Z-number) | Z-2073-2021 |
|---|---|
| Recall event | 88127 |
| Product | Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an assist ventilator and is intended to augment patient breathing. It is intended for spontaneously breathing individuals who require mechanical ventilation: patients with respiratory… |
| Product code | MNT |
| Recalling firm | Respironics California, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2518422 |
At a glance
- None 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