BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES OBS10/25/04

    MDR report key: 2119556 · Received May 27, 2011

    Report

    Report Number
    1831750-2011-05241
    Event Type
    Malfunction
    Date Received
    May 27, 2011
    Date of Event
    May 2, 2011
    Report Date
    May 2, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FAULTY HEAD-END HYD HACK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD-END WILL NOT RAISE OR LOWER. THERE WAS NO REPORTED FLUID FOUND ON FLOOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT SERIES OBS10/25/04 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0721 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK