BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ERBE FLEXIBLE CRYOPROBE

    MDR report key: 24270426 · Received February 5, 2026

    Report

    Report Number
    9610614-2026-00024
    Event Type
    Malfunction
    Date Received
    February 5, 2026
    Date of Event
    January 14, 2026
    Report Date
    February 5, 2026
    Manufacturer
    ERBE ELEKTROMEDIZIN GMBH
    Product Code
    GEH
    PMA / PMN Number
    K190651
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE CRYOPROBE WAS EVALUATED BY ERBE USA ON 2026-02-05. THE VISUAL EXAMINATION REVEALED THAT THERE WAS A SLIT OR CUT IN THE WHITE TUBING APPROXIMATELY 18MM LONG AND LOCATED 16.1CM FROM THE DISTAL END OF THE WHITE TUBING. THEN AT THE DIRECTION OF THE MANUFACTURER, ERBE ELEKTROMEDIZIN GMBH (ERBE GERMANY), THE CRYOPROBE'S CONNECTOR SECTION WAS DISASSEMBLED AS INSTRUCTED. GLUE BETWEEN THE CONNECTOR AND THE CLEAR PLASTIC TUBING ON THE HIGH-PRESSURE SIDE OF THE CRYOPROBE WAS FOUND TO BE INSUFFICIENT. THE HIGH-PRESSURE TUBING WAS ALSO PUSHED OUT OF THE CONNECTOR, AND THE BLUE O-RING WAS STILL PRESENT. NO ANOMALIES WERE FOUND IN THE REVIEW OF THE DEVICE HISTORY RECORD (DHR) FOR THE LOT OF THE CRYOPROBE. ASSESSMENT BY ERBE GERMANY ERBE HAS BEEN MADE AWARE OF ISOLATED CASES WHERE THE OUTER WHITE TUBING OF CRYOPROBES RUPTURE. AFTER A THOROUGH INVESTIGATION, IT HAS BEEN CONCLUDED THAT A VERY LOW NUMBER OF ISOLATED INCIDENTS HAVE OCCURRED INVOLVING THE REPORTED FAILURE MODE. MORE SPECIFICALLY, LESS THAN 0.1% OF CRYOPROBES MANUFACTURED DURING THE TIMEFRAME WHICH THE PROBLEM WAS DISCOVERED HAVE RUPTURED. IN THESE RARE CASES, THE FIXATION OF THE GAS INLET INSIDE THE PROBE CONNECTOR HAD LOOSENED, ALLOWING GAS TO FLOW INTO THE RETURN LINE. SINCE THE RETURN LINE IS NOT DESIGNED FOR THIS VOLUME OF GAS, THE TUBING COULD RUPTURE. SINCE DISCOVERING THE ISSUE, THE MANUFACTURING PROCESS HAS BEEN IMPROVED BY STABILIZING THE ADHESIVE APPLICATION AND ADDING ADDITIONAL VISUAL INSPECTION STEPS TO MONITOR THE GLUING OF EACH CRYOPROBE. ALL OF THESE MEASURES HAVE BEEN IMPLEMENTED TO MINIMIZE/ELIMINATE THE ISSUE. THE CUSTOMER IS BEING MADE AWARE OF THE FINDINGS. ERBE USA, INC. IS CLOSING THE FILE ON THIS EVENT.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT AN INCIDENT OCCURRED WITH A FLEXIBLE CRYOPROBE. THE CRYOPROBE WAS USED WITH AN ERBE CRYOSURGICAL UNIT (MODEL ERBECRYO 2, PART NUMBER: 10402-000, SERIAL NUMBER: NOT PROVIDED) AND ION ROBOTIC NAVIGATIONAL SYSTEM. NO OTHER INFORMATION WAS PROVIDED REGARDING ANY OTHER ACCESSORY EMPLOYED DURING THE EVENT. THE CRYOSURGICAL UNIT'S SETTING WAS 56 BAR. PER THE ACCOUNT, THEY HEARD A LEAKING SOUND, BUT TOOK A BIOPSY WITHOUT ANY ISSUES. ONCE ACTIVATING AGAIN, THE CRYOPROBE POPPED IN THE RTS HAND (NOTE: THE CRYOPROBE WAS NOT IN THE PATIENT'S BODY.). THERE WAS NO REPORT OF ANY INJURY TO THE STAFF OR PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    332363 ERBE FLEXIBLE CRYOPROBE CRYOPROBE GEH ERBE ELEKTROMEDIZIN GMBH

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Unknown