Device recall
Z-1177-2013: Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator…
FDA device recall · Class I · Maquet Cardiovascular Us Sales, Llc
Key facts
| Recall number (Z-number) | Z-1177-2013 |
|---|---|
| Recall event | 64645 |
| Product | Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180). Battery for use with the SERVO-i Ventilator System. The SERVO-i Ventilator System is intended for treating and monitoring patients ranging from neonates to adults with respiratory failure or… |
| Product code | CBK |
| Recalling firm | Maquet Cardiovascular Us Sales, Llc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 11, 2016 |
| 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