Device recall
Z-1385-2022: HAMILTON-H900 Humidifier, Models: 950001, 950004
FDA device recall · Class III · Hamilton Medical AG
Key facts
| Recall number (Z-number) | Z-1385-2022 |
|---|---|
| Recall event | 90460 |
| Product | HAMILTON-H900 Humidifier, Models: 950001, 950004 |
| Product code | BTT |
| Recalling firm | Hamilton Medical AG |
| Recall class | Class III |
| Status | Completed |
| 510(k) numbers | K163283 |
| FEI number | 3001421318 |
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