BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RUSCH GREENSPEC STUBBY LARYNGOSCOPE HANDLE

    MDR report key: 2021322 · Received February 7, 2011

    Report

    Report Number
    3004365956-2011-00055
    Event Type
    Malfunction
    Date Received
    February 7, 2011
    Date of Event
    January 12, 2011
    Report Date
    January 14, 2011
    Manufacturer
    TELEFLEX MEDICAL
    Product Code
    CCW
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SAMPLE RECEIVED BY MFR. THE RESULTS OF THE INVESTIGATION ARE NOT AVAILABLE AT THE TIME OF THIS REPORT. A F/U REPORT WILL BE SENT WHEN COMPLETED.

    Description of Event or Problem · 1

    EVENT REPORTED AS: THE LARYNGOSCOPE HANDLE GOT HOT TO TOUCH WHEN BATTERIES WERE PLACED INSIDE. NO HEALTHCARE PROFESSIONAL INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RUSCH GREENSPEC STUBBY LARYNGOSCOPE HANDLE STUBBY LARYNGOSCOPE HANDLE CCW TELEFLEX MEDICAL NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK