Device recall
Z-2141-2023: HAMILTON C2 Ventilator Is intended to provide positive pressure ventilatory…
FDA device recall · Class I · Hamilton Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2141-2023 |
|---|---|
| Recall event | 92482 |
| Product | HAMILTON C2 Ventilator Is intended to provide positive pressure ventilatory support to adults and pediatrics, and optionally infants and neonates |
| Product code | CBK |
| Recalling firm | Hamilton Medical, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K121225 |
| FEI number | 2937708 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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