International safety notice
Linvatec recalls the PowerPro® Electric II Modular Handpiece
Germany / BfArM · DEU · Jul 14, 2005
Key facts
| Title | Linvatec recalls the PowerPro® Electric II Modular Handpiece |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Linvatec recalls the PowerPro® Electric II Modular Handpiece |
| Manufacturer | Linvatec recalls the PowerPro® Electric II Modular Handpiece |
| Models | 800-237-0169, P4001, PR06100, 727-392-6464 |
| Date | Jul 14, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1