Device recall
Z-2418-2020: Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD; 30004 LokomatPro…
FDA device recall · Class II · Hocoma AG
Key facts
| Recall number (Z-number) | Z-2418-2020 |
|---|---|
| Recall event | 85857 |
| Product | Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2 120V PE; 30683 LokomatPro L6.2 110V FD PE; 30684 LokomatPro L6.2 110V FD Kombi; 32001 LokomatPro L6.2 110V FD AD Product Usage: The intended use of the Lokomat is to support treadmill… |
| Product code | IKK |
| Recalling firm | Hocoma AG |
| Recall class | Class II |
| Status | Open, Classified |
| 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