Device recall
Z-1208-2009: Screwdriver for 3.5mm Screws, DARCO system, instrument for use in orthopaedic…
FDA device recall · Class II · Wright Medical Technology Inc
Key facts
| Recall number (Z-number) | Z-1208-2009 |
|---|---|
| Recall event | 51431 |
| Product | Screwdriver for 3.5mm Screws, DARCO system, instrument for use in orthopaedic implant surgery. REF: DC4261, Non-sterile, Rx only, 1 each, Wright Medical Technology, Inc., 5677 Airline, Road, Arlington, TN 38002 |
| Product code | LXH |
| Recalling firm | Wright Medical Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 3, 2010 |
| FEI number | 1043534 |
At a glance
- None 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