Device recall
Z-0879-2017: OrthoPediatrics PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical…
FDA device recall · Class III · OrthoPediatrics Corp
Key facts
| Recall number (Z-number) | Z-0879-2017 |
|---|---|
| Recall event | 75758 |
| Product | OrthoPediatrics PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screw |
| Product code | HSB |
| Recalling firm | OrthoPediatrics Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2017 |
| 510(k) numbers | K083726 |
| FEI number | 3006460162 |
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