Device recall
Z-2442-2008: SERVO-i Ventilator System Maquet Critical Care, Solna, Sweden. The product is…
FDA device recall · Class II · MAQUET Inc.
Key facts
| Recall number (Z-number) | Z-2442-2008 |
|---|---|
| Recall event | 49117 |
| Product | SERVO-i Ventilator System Maquet Critical Care, Solna, Sweden. The product is intended for treatment and monitoring of patients in the range of neonates, infants and adults with respiratory failure or respiratory insufficiency. |
| Product code | CBK |
| Recalling firm | MAQUET Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2008 |
| 510(k) numbers | K041223 |
| FEI number | 3008355164 |
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