Lutronic Recalls

2 recalls found for Lutronic. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Lutronic CLARITY II Laser System Recalled for 1,525 Units Worldwide in 2026

Lutronic's CLARITY II Laser System, 1,525 units distributed worldwide to US clinics and international markets, is recalled. The devices have reports of sparking and popping during use and may burn patients. Clinics and patients should stop using the device immediately and follow the manufacturer's recall instructions.

Lutronic
Reports of
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Health & Personal Care
HIGH
FDA DEVICE

Lutronic XERF EFFECTOR 60 Electrosurgical Unit Recalled for Manufacturing Defects (2025-2026 Models)

Lutronic recalled 7,490 XERF EFFECTOR 60 electrosurgical units distributed worldwide, including several U.S. states, after manufacturing defects surfaced between April 1 and August 20, 2025. The defect can cause adverse events for patients. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.

Lutronic
Manufacturing defects
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Brand Statistics

Total Recalls
2
Pages
1

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