Device recall
Z-0952-2013: Extremity Medical - Disposable Orthopedic Surgical Instrument - 1.6 mm Guidewire…
FDA device recall · Class II · Extremity Medical LLC
Key facts
| Recall number (Z-number) | Z-0952-2013 |
|---|---|
| Recall event | 64330 |
| Product | Extremity Medical - Disposable Orthopedic Surgical Instrument - 1.6 mm Guidewire - Reference Number 101-00006 - Non-Sterile. Contained in Extremity Medical Surgical Kits including CompressX, Hallu.X, IO Fix and XMCP. Used in the selection of screw size when used with appropriate depth gauge. |
| Product code | HXI |
| Recalling firm | Extremity Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2013 |
| FEI number | 3007289093 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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