Device recall
Z-2722-2011: Pathfinder NXT Closure top driver - long, REF 3566-1, Zimmer Inc., Warsaw, IN…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-2722-2011 |
|---|---|
| Recall event | 58536 |
| Product | Pathfinder NXT Closure top driver - long, REF 3566-1, Zimmer Inc., Warsaw, IN Product Usage: The Closure Top Driver is used in conjunction with compressors, distractors, and reducers, as needed, to manipulate and hold the spine into the desired position via loosening/tightening maneuvers on the… |
| Product code | HXX |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2011 |
| 510(k) numbers | K100845 |
| FEI number | 1000220733 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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