The Thuvera Laser Console, a portable thulium fiber laser platform used for skin resurfacing and soft-tissue procedures, has been recalled due to a software defect in version 2.2. Thulium lasers operate at 1940 nm, targeting water in tissue for ablative and fractional treatments—popular for fine lines, texture, and pigmentation work.
If you own a Thuvera unit, the software issue could compromise treatment parameters or console performance during procedures. IPG Medical Corporation issued the recall in early May. Check your device's software version immediately; if it's 2.2, contact IPG for instructions on a patch or replacement.
Portable laser consoles appeal to practices with multiple treatment rooms or mobile service models, but software reliability is non-negotiable when you're working on a patient's face. Confirm your unit's status before your next session.
See the official FDA recall notice for device identifiers and next steps.
View the official FDA record ↗
This post summarizes a public FDA database entry for medical-aesthetics owners. It is general business information, not medical, legal, or regulatory advice. Always confirm scope, lot numbers, and classification against the official FDA record, and consult your own clinician or counsel for anything clinical or compliance-related.