Device recall
Z-0158-2007: Jostra - HL-20 Heart Lung Integrated Perfusion System, Roller Pump Hand crank
FDA device recall · Class II · MAQUET Inc.
Key facts
| Recall number (Z-number) | Z-0158-2007 |
|---|---|
| Recall event | 36252 |
| Product | Jostra - HL-20 Heart Lung Integrated Perfusion System, Roller Pump Hand crank |
| Product code | DTQ |
| Recalling firm | MAQUET Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 19, 2007 |
| 510(k) numbers | K943803 |
| 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