Device recall
Z-2238-2011: Maquet Magnus Carbon-fibre table top; Device Part Number 1180.16xx (x represents…
FDA device recall · Class II · Maquet Inc.
Key facts
| Recall number (Z-number) | Z-2238-2011 |
|---|---|
| Recall event | 58789 |
| Product | Maquet Magnus Carbon-fibre table top; Device Part Number 1180.16xx (x represents a digit from 0-5 and F-for the US market) The carbon-fibre MAGNUS table top serves to support and position patients for surgical procedures and interventional examination immediately before, during and after the… |
| Product code | KXJ |
| Recalling firm | Maquet Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2013 |
| 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