Device recall
Z-1951-2009: PowerProMax PRO5100M Battery Single Trigger, PowerProMax PRO5200M Battery Two…
FDA device recall · Class I · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-1951-2009 |
|---|---|
| Recall event | 52803 |
| Product | PowerProMax PRO5100M Battery Single Trigger, PowerProMax PRO5200M Battery Two Trigger, PowerProMax PRO5250M Battery Two-Trigger Standard, PowerProMax PRO5300M Battery Oscillator, PowerProMax PRO5400M Battery Reciprocator, and PowerProMax PRO6200 Battery Single Trigger. CONMED LINVATEC, 11311 CONCEPT… |
| 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