Lutronic Corporation
Lutronic Corporation: 2 recalls listed since March 2026 across FDA.
By year
- 20262
By agency
- FDA2
By category
- Medical Device2
All recalls (2)
Lutronic DermaV Laser System
Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.
Lutronic CLARITY II Laser System
The Clarity II Laser System can spark or pop and potentially burn patients.
