Device recall
Z-0623-2014: Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN…
FDA device recall · Class II · Aesculap, Inc.
Key facts
| Recall number (Z-number) | Z-0623-2014 |
|---|---|
| Recall event | 67050 |
| Product | Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN and microspeed motor systems to hold burrs which cut and shape bone. |
| Product code | GET |
| Recalling firm | Aesculap, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 2, 2014 |
| FEI number | 2916714 |
At a glance
- None 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