BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SM304 M-SERIES W/ZOOM

    MDR report key: 1760087 · Received July 9, 2010

    Report

    Report Number
    1831750-2010-01479
    Event Type
    Malfunction
    Date Received
    July 9, 2010
    Date of Event
    June 30, 2010
    Report Date
    June 30, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    INK
    PMA / PMN Number
    K022309
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: DAMPNER.

    Description of Event or Problem · 1

    IT WAS REPORTED IN (B)(4) THAT THERE IS OIL LEAKING FROM THE STRETCHER. NO ADVERSE CONSEQUENCES ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM304 M-SERIES W/ZOOM WHEELED POWERED STRETCHER INK STRYKER CORP., MEDICAL DIVISION 1025

    Patients

    Seq Age Sex Outcome Treatment
    1 NA