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IPG Medical Corporation recalls Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Recalled July 1, 2026 · FDA recall Z-2554-2026 · IPG Medical
Hazard
Software anomaly that causes a false display of error code 5018. · FDA Class II
Units
198 units
Sold at
US Nationwide distribution in the state of MA.
Description
Software anomaly that causes a false display of error code 5018.
Product
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Manufacturer(s)
IPG Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →