Device recall
Z-0917-2013: D3000I Advantage Drive System, 230v, surgical instrument motor. Product Usage…
FDA device recall · Class III · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-0917-2013 |
|---|---|
| Recall event | 64367 |
| Product | D3000I Advantage Drive System, 230v, surgical instrument motor. Product Usage: The Advantage Drive Systems function as a powered instrument system consisting of handpieces and accessories to perform cutting of soft tissue and bone |
| Product code | GEY |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 5, 2013 |
| 510(k) numbers | K050519 |
| FEI number | 1017294 |
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