Device recall
Z-0021-05: Stryker Navigation System - Hip Module Patient Tracker, blue; Model…
FDA device recall · Class II · Stryker Instruments, Instruments Div.
Key facts
| Recall number (Z-number) | Z-0021-05 |
|---|---|
| Recall event | 29675 |
| Product | Stryker Navigation System - Hip Module Patient Tracker, blue; Model 6007-010-000. |
| Product code | HAW |
| Recalling firm | Stryker Instruments, Instruments Div. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2004 |
| 510(k) numbers | K022365 |
| FEI number | 1811755 |
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