Device recall
Z-2445-2008: Universal Optical Tracker Fixation, not sterile, Manufactured by Orthosoft…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-2445-2008 |
|---|---|
| Recall event | 49122 |
| Product | Universal Optical Tracker Fixation, not sterile, Manufactured by Orthosoft, Montreal, Canada, REF 111.031. Surgical instrument. |
| Product code | HAW |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 11, 2009 |
| 510(k) numbers | K030827 |
| FEI number | 1000220733 |
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