Class II

Medical Device Recall: Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

IPG Medical Corporation · May 5, 2026

Reason for Recall

Software anomaly that causes a false display of error code 5018.

Distribution

US Nationwide distribution in the state of MA.

States Affected

NATIONWIDE

Quantity Affected

198 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2554-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.