Health & Personal Care
HIGH
FDA DEVICE
Lutronic CLARITY II Laser System Recalled for 1,525 Units Worldwide in 2026
Reports of devices sparking/popping and potentially burning patients.
Lutronic
Reports of
Brand hub
Reports of devices sparking/popping and potentially burning patients.
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.