Device recall
Z-0525-2010: Abbott Spine Thoracolumbar Common, SpdLnk 5.5 Trans Cntr Med 43-51 mm…
FDA device recall · Class III · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0525-2010 |
|---|---|
| Recall event | 53454 |
| Product | Abbott Spine Thoracolumbar Common, SpdLnk 5.5 Trans Cntr Med 43-51 mm, non-sterile, Manufactured by Abbott Spine, Inc., Austin, TX; Ref. 1302-55M. Note: This lot was not distributed in the United States. The component is used in the stabilization of constructs in the BacFix and InCompass spinal… |
| Product code | KWP |
| Recalling firm | Zimmer Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 8, 2010 |
| 510(k) numbers | K002082 |
| 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