Device recall
Z-1252-2009: Servo Ventilator 300 (Model SV300) and Servo Ventilator 300 (Model SV300A). The…
FDA device recall · Class II · MAQUET Inc.
Key facts
| Recall number (Z-number) | Z-1252-2009 |
|---|---|
| Recall event | 51473 |
| Product | Servo Ventilator 300 (Model SV300) and Servo Ventilator 300 (Model SV300A). The SV300 is intended for general and critical ventilatory care for use on adults, pediatric, infant and neonatal patients. The unit is designed to be used at the bedside for intra-hospital transport. |
| Product code | CBK |
| Recalling firm | MAQUET Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2009 |
| 510(k) numbers | K902859, K970839 |
| 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