HIGH
FDA DEVICE
CLARITY II Laser System; Model No. 1110200210.
Reports of devices sparking/popping and potentially burning patients.
Lutronic
Reports of
Lutronic Recalls
2 recalls found for Lutronic. Check if any of your products are affected.
Health & Personal Care
HIGH
FDA DEVICE
Lutronic Recalls Electrosurgical Unit Due to Defect Risks
Lutronic recalled 7,490 units of the XERF EFFECTOR 60 electrosurgical unit on September 4, 2025. Manufacturing defects may lead to adverse events for patients. Devices manufactured between April 1, 2025, and August 20, 2025, are affected.
Lutronic
Manufacturing defects
Brand Statistics
Total Recalls
2
Pages
1