Device recall
Z-1819-2015: ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN 69-1012. Drill…
FDA device recall · Class II · Orthofix, Inc
Key facts
| Recall number (Z-number) | Z-1819-2015 |
|---|---|
| Recall event | 71262 |
| Product | ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN 69-1012. Drill Guides are used to interface with various drill tips during the drilling procedure of bone preparation. |
| Product code | FZX |
| Recalling firm | Orthofix, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 17, 2016 |
| FEI number | 2183449 |
At a glance
- None 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