Device recall
Z-0075-2011: Pathfinder End Screw Extender Sleeve, REF 1165-10, Rx, non-sterile, sold under…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0075-2011 |
|---|---|
| Recall event | 54550 |
| Product | Pathfinder End Screw Extender Sleeve, REF 1165-10, Rx, non-sterile, sold under label Abbott Spine, Inc. Austin TX (prior to 2008) and Zimmer Spine Austin TX (7/2009 to present) |
| Product code | NKB |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 2012 |
| 510(k) numbers | K030625 |
| 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