BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COMPACT AIR DRIVE II

    MDR report key: 4102339 · Received September 19, 2014

    Report

    Report Number
    8030965-2014-01455
    Event Type
    Malfunction
    Date Received
    September 19, 2014
    Report Date
    February 7, 2013
    Manufacturer
    SYNTHES GMBH
    Product Code
    HWE
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO SYNTHES OUS SERVICE AND REPAIR FILES LEGACY REVIEW/REMEDIATION PROTOCOL-COMPLAINT HANDLING AND MDR REPORTING. DEVICE LISTED IN THIS REPORT IS USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. DURING PRE-REPAIR ASSESSMENT PERFORMED BY A TECHNICIAN, IT WAS REVEALED THAT THE INVERSE TRIGGER WAS BLOCKED, THE DEVICE LACKS LUBRICATION, AND IS DIRTY DUE TO LACK OF CLEANING. THE DEVICE WAS REPAIRED AND RETURNED TO THE CUSTOMER ON (B)(6) 2013. PLACEHOLDER.

    Description of Event or Problem · 1

    NO ERROR DESCRIPTION WAS SENT WITH THE RETURNED DEVICE. DURING THE INSPECTION THE TECHNICIAN NOTED THE MOTOR HAS THE INVERSE TRIGGER BLOCKED. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    584188 COMPACT AIR DRIVE II HWE SYNTHES GMBH 1903

    Patients

    Seq Age Sex Outcome Treatment
    1