Device recall
Z-0082-2014: MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012…
FDA device recall · Class II · Maquet Medical Systems USA
Key facts
| Recall number (Z-number) | Z-0082-2014 |
|---|---|
| Recall event | 66336 |
| Product | MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG Made in Germany. Cardiopulmonary support system. |
| Product code | DTQ |
| Recalling firm | Maquet Medical Systems USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2017 |
| 510(k) numbers | K102726 |
| 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