Device recall
Z-2075-2017: Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument
FDA device recall · Class III · Orthosoft, Inc. dba Zimmer CAS
Key facts
| Recall number (Z-number) | Z-2075-2017 |
|---|---|
| Recall event | 75612 |
| Product | Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument |
| Product code | HAW |
| Recalling firm | Orthosoft, Inc. dba Zimmer CAS |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 15, 2017 |
| 510(k) numbers | K060336 |
| FEI number | 3003714383 |
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