Device recall
Z-1008-2007: Anspach Single Use, Sterile Bone Cutting Burrs
FDA device recall · Class II · The Anspach Effort, Inc.
Key facts
| Recall number (Z-number) | Z-1008-2007 |
|---|---|
| Recall event | 37977 |
| Product | Anspach Single Use, Sterile Bone Cutting Burrs |
| Product code | HBB |
| Recalling firm | The Anspach Effort, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 17, 2009 |
| 510(k) numbers | K011444, K061297, K955084, K965080 |
| FEI number | 1045834 |
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