Day

June 24, 2026
24
Jun

FDA Recall: Software anomaly that causes a false display of error code 5018

June 24, 2026
Company: IPG Medical Corporation Date of Enforcement Report: 6/24/2026 Class: II PRODUCT: Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser. Recall Number: Z-2554-2026 REASON: Software anomaly that causes a false display of error code 5018. RECALLING FIRM/MANUFACTURER: IPG Medical Corporation VOLUME: 198 units DISTRIBUTION: US Nationwide distribution in the state of MA.
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