Device recall
Z-0435-2021: OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails
FDA device recall · Class II · Merete Medical GmbH
Key facts
| Recall number (Z-number) | Z-0435-2021 |
|---|---|
| Recall event | 86526 |
| Product | OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails |
| Product code | HSB |
| Recalling firm | Merete Medical GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 13, 2021 |
| 510(k) numbers | K101939 |
| FEI number | 3002949614 |
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