Device recall
Z-0590-2010: Hocoma Lokomat-System with Pediatric Module Software Versions: V4.30, V4.31…
FDA device recall · Class II · Hocoma AG
Key facts
| Recall number (Z-number) | Z-0590-2010 |
|---|---|
| Recall event | 52207 |
| Product | Hocoma Lokomat-System with Pediatric Module Software Versions: V4.30, V4.31, V4.31a, V4.31b, V4.31c, V4.32, V4.32a, V5.0x. Powered exercise equipment used to apply automated locomoter training for hemiplegic and paraplegic patients. |
| Product code | BXB |
| Recalling firm | Hocoma AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2010 |
| FEI number | 3003781275 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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