Class IIOngoingZ-1558-2026
Lutronic Corporation recalls CLARITY II Laser System
Reports of devices sparking/popping and potentially burning patients.
Lutronic CorporationMar 18, 2026
Lutronic Corporation recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–2 of 2 recalls
Class IIOngoingZ-0146-2026
Lutronic Corporation recalls XERF EFFECTOR 60. Electrosurgical unit.
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.
Lutronic CorporationOct 22, 2025