Device recall
Z-1950-2009: PRO5100, PowerPro Battery Modular Handpiece. Drill mode Nominal Speed Range…
FDA device recall · Class I · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-1950-2009 |
|---|---|
| Recall event | 52803 |
| Product | PRO5100, PowerPro Battery Modular Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5200, PowerPro Battery Two Trigger Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5250, PowerPro Battery Two Trigger Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5300 PowerPro Battery… |
| Product code | HRX |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 19, 2011 |
| 510(k) numbers | K981269 |
| 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