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Medical Device

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

Recall date: 2026-07-01 · Source: FDA_DEVICE
Brand / Firm
IPG Medical Corporation
Product
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Reason for recall
Software anomaly that causes a false display of error code 5018.
Units affected
198 units
Description
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
View official recall notice →