Device recall
Z-2210-2012: Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler…
FDA device recall · Class II · Maquet Inc.
Key facts
| Recall number (Z-number) | Z-2210-2012 |
|---|---|
| Recall event | 62471 |
| Product | Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 [email protected] www.maquet.com Used to introduce blood and sterile solution to the circulation system during extracorporeal circulation… |
| Product code | NCP |
| Recalling firm | Maquet Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 3, 2014 |
| 510(k) numbers | K023251 |
| FEI number | 3008355164 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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