BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER INSTRUMENT

    MDR report key: 239732 · Received September 8, 1999

    Report

    Report Number
    MW1017141
    Event Type
    Malfunction
    Date Received
    September 8, 1999
    Date of Event
    August 27, 1999
    Report Date
    September 8, 1999
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    HWE
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PROCEDURE - BUNIONECTOMY. SAW BLADE CAME LOOSE IN OPERATION AND PIN CAME OUT AND OIL WAS LEAKING ON DR'S GLOVES. NO HARM TO PT PER PHYSICIAN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER INSTRUMENT MICRO ELECTRIC SAG SAW HWE STRYKER INSTRUMENTS 2296-234 *

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Other