Device recall
Z-1952-2009: Mpower PRO6200 Single Trigger Modular Handpiece, Mpower PRO6202 Battery…
FDA device recall · Class I · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-1952-2009 |
|---|---|
| Recall event | 52803 |
| Product | Mpower PRO6200 Single Trigger Modular Handpiece, Mpower PRO6202 Battery Two-Trigger Modular Handpiece, Mpower PRO6300 Battery Oscillating Saw, Mpower PRO6400 Battery Reciprocating Saw, and Mpower PRO6450 Battery Sternum Saw. CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA. |
| 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