Device recall
Z-0538-2024: AirTouch F20 Full Face Mask and User Guide
FDA device recall · Class I · ResMed Ltd.
Key facts
| Recall number (Z-number) | Z-0538-2024 |
|---|---|
| Recall event | 93499 |
| Product | AirTouch F20 Full Face Mask and User Guide |
| Product code | BZD |
| Recalling firm | ResMed Ltd. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K153563 |
| FEI number | 3004604967 |
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