Device recall
Z-0176-2010: RESPIRONICS V60 VENTILATOR
FDA device recall · Class II · Respironics California Inc
Key facts
| Recall number (Z-number) | Z-0176-2010 |
|---|---|
| Recall event | 53676 |
| Product | RESPIRONICS V60 VENTILATOR |
| Product code | MNT |
| Recalling firm | Respironics California Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2011 |
| 510(k) numbers | K082660 |
| 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