Device recall
Z-0041-05: Ultra Power Burs, Sterile, Single-Use.
FDA device recall · Class II · Linvatec Corp.
Key facts
| Recall number (Z-number) | Z-0041-05 |
|---|---|
| Recall event | 29916 |
| Product | Ultra Power Burs, Sterile, Single-Use. |
| Product code | HRX |
| Recalling firm | Linvatec Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 2012 |
| 510(k) numbers | K781979 |
| FEI number | 1017294 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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