Device recall
Z-1687-2017: Philips V60 Ventilator with Version 2.20 Software, Description: V 60…
FDA device recall · Class II · Respironics California Inc
Key facts
| Recall number (Z-number) | Z-1687-2017 |
|---|---|
| Recall event | 76377 |
| Product | Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ventilator,Intl Opt: CFLEX,AVAPS,PPV V60 Ventilator,Intl Opt: CFLEX,AVAPS V60 Ventilator,Intl Opt: None V60 Ventilator,English Opt: None V60 Ventilator,Engl Opt: CFLEX,AVAPS V60 Us Demo Unit V60 USED ENGL OPT:CFLEX, AVAPS,PPV,AT+cl… |
| Product code | MNT |
| Recalling firm | Respironics California Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2018 |
| 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