Device recall
Z-0721-2022: NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
FDA device recall · Class II · Orthosoft, Inc. dba Zimmer CAS
Key facts
| Recall number (Z-number) | Z-0721-2022 |
|---|---|
| Recall event | 89619 |
| Product | NavitrackER Kit A: Knee, Model Number 20-8000-000-07, |
| Product code | OLO |
| Recalling firm | Orthosoft, Inc. dba Zimmer CAS |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K110054 |
| 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