Device recall
Z-1430-2012: Double foot switch, type KF 2 1S/1 S-MED-AP, manufactured by the company Seute…
FDA device recall · Class II · Ziehm Imaging Inc
Key facts
| Recall number (Z-number) | Z-1430-2012 |
|---|---|
| Recall event | 60661 |
| Product | Double foot switch, type KF 2 1S/1 S-MED-AP, manufactured by the company Seute Schaltgerate. GmbH & Co. KG for Ziehm Imaging GmbH Germany, and used with Ziehm Imaging GmbH Mobile C-arm as a component thereof. Two versions were made: 2 pedal version KF 2 1S/1 S-MED-AP foot switch and 4 pedal foot… |
| Product code | JAA |
| Recalling firm | Ziehm Imaging Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 18, 2012 |
| 510(k) numbers | K061203, K073346, K083545, K092438 |
| FEI number | 2027299 |
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