Device recall
Z-0884-2020: Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth, Diameter 2.8 mm…
FDA device recall · Class II · Brasseler USA I Lp
Key facts
| Recall number (Z-number) | Z-0884-2020 |
|---|---|
| Recall event | 84545 |
| Product | Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth, Diameter 2.8 mm, Length 228 mm Product Usage: A Steinmann Pin is used for internal fixation of large bone fractures. |
| Product code | HTY |
| Recalling firm | Brasseler USA I Lp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2021 |
| 510(k) numbers | K945670 |
| FEI number | 3004949275 |
At a glance
- 1–9 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