Device recall
Z-0620-2009: Foot switch, Part Number 1009.81. Maquet GmbH & Co. KG, 76437 Rastatt, Germany…
FDA device recall · Class II · MAQUET Inc.
Key facts
| Recall number (Z-number) | Z-0620-2009 |
|---|---|
| Recall event | 50472 |
| Product | Foot switch, Part Number 1009.81. Maquet GmbH & Co. KG, 76437 Rastatt, Germany. The foot switches in the 1009.8 1 series are accessory components which can be connected to certain MAQUET operating tables. Several of the table top adjustment motions (depending on the table and foot switch versions in… |
| Product code | FWZ |
| Recalling firm | MAQUET Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 18, 2012 |
| FEI number | 3008355164 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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