Device recall
Z-1474-2011: Aesculap MicroSpeed Uni Control Box, Part #GD670 Intended for high speed…
FDA device recall · Class II · Aesculap Inc
Key facts
| Recall number (Z-number) | Z-1474-2011 |
|---|---|
| Recall event | 57419 |
| Product | Aesculap MicroSpeed Uni Control Box, Part #GD670 Intended for high speed cutting, sawing, drilling and manipulation of soft tissue and bone in the fields of Spine, ENT, Neuro and Maxillo facial Surgery. |
| Product code | HBC |
| Recalling firm | Aesculap Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 5, 2012 |
| 510(k) numbers | K053526 |
| FEI number | 2916714 |
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