https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218672
Class 2 Device Recall Olympus SOLTIVE Pro SuperPulsed Laser System
device recallclassolympusprolaser
https://www.igj.nl/documenten/fsn-2026/03/18/gyrus-acmi-inc.-olympus-europa-se-and-co.-kg-qil-fy26-emea-25-fy26-049-soltive-laser-system
Gyrus ACMI, Inc., QIL FY26-EMEA-25-FY26-049, Soltive Laser System | Inspectie Gezondheidszorg en...
Olympus has received ninety-eight (98) complaints describing an abrupt loss of power and functionality of the SOLTIVE SuperPulsed Laser System, or an inability...