Device recall
Z-1536-2009: TransFx External Fixation System Drill Bit, Quick Connect, 4.0 mm diameter, 195…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-1536-2009 |
|---|---|
| Recall event | 51924 |
| Product | TransFx External Fixation System Drill Bit, Quick Connect, 4.0 mm diameter, 195 mm length, nonsterile, Zimmer, Warsaw, IN; REF 4450-63. TransFx drill bits can be found in the following kits: TransFx Intermediate External Fixation System, REF 4450-05-10; TransFx Large External Fixation System, REF… |
| Product code | LXT |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2010 |
| 510(k) numbers | K003205, K984357, K990848, K991723 |
| 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