Device recall
Z-3057-2011: Maquet HL Console for Heart Lung Machine HL20: HL 20 4-pumps console base: P/N…
FDA device recall · Class II · Maquet Inc.
Key facts
| Recall number (Z-number) | Z-3057-2011 |
|---|---|
| Recall event | 59576 |
| Product | Maquet HL Console for Heart Lung Machine HL20: HL 20 4-pumps console base: P/N 917741 HL 20 5-pumps console base: P/N 917751 The HL 20 is indicated for use as an extracorporeal circulation device for perfusion lasting not more then six hours. The HL console is equipped with a rack for accommodating… |
| Product code | DTQ |
| Recalling firm | Maquet Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 16, 2012 |
| 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