Device recall
Z-1363-2018: ORTHOFIX, Connector System, SMALL SET SCREW, REF 79-2003
FDA device recall · Class II · Orthofix, Inc
Key facts
| Recall number (Z-number) | Z-1363-2018 |
|---|---|
| Recall event | 79498 |
| Product | ORTHOFIX, Connector System, SMALL SET SCREW, REF 79-2003 |
| Product code | NKG |
| Recalling firm | Orthofix, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 18, 2019 |
| 510(k) numbers | K172194 |
| FEI number | 2183449 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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