Device recall
Z-1537-2013: Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 12…
FDA device recall · Class I · Respironics California Inc
Key facts
| Recall number (Z-number) | Z-1537-2013 |
|---|---|
| Recall event | 65376 |
| Product | Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 12 Digit P/N): 85008 (85008) 1053613 (989805628251) 1053614 (989805612101) 1053615 (989805613391) 1053616 (989805613661) 1053617 (989805611761) 1053618 (n/a) R1053618 (n/a) 1076709 (n/a) 1076715 (989805627411) 1076716… |
| Product code | MNT |
| Recalling firm | Respironics California Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 24, 2014 |
| 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