Device recall
Z-1678-2022: Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
FDA device recall · Class II · OrthoPediatrics Corp
Key facts
| Recall number (Z-number) | Z-1678-2022 |
|---|---|
| Recall event | 90738 |
| Product | Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN |
| Product code | KTT |
| Recalling firm | OrthoPediatrics Corp |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K151881 |
| FEI number | 3006460162 |
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