Device recall
Z-2260-2012: V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usage: The…
FDA device recall · Class I · Respironics California Inc
Key facts
| Recall number (Z-number) | Z-2260-2012 |
|---|---|
| Recall event | 62848 |
| Product | V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usage: The V60 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 failure… |
| Product code | MNT |
| Recalling firm | Respironics California Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 22, 2013 |
| 510(k) numbers | K082660, 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