Device recall
Z-2550-2016: Quattro Air FFM MED AMER, Product Code: 62702, full face mask for use with…
FDA device recall · Class II · Resmed Corporation
Key facts
| Recall number (Z-number) | Z-2550-2016 |
|---|---|
| Recall event | 74736 |
| Product | Quattro Air FFM MED AMER, Product Code: 62702, full face mask for use with active-exhaust-valve ventilators |
| Product code | BZD |
| Recalling firm | Resmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 26, 2016 |
| 510(k) numbers | K123979 |
| FEI number | 1000115734 |
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