BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADEL OBS

    MDR report key: 2914271 · Received December 6, 2012

    Report

    Report Number
    1831750-2012-12345
    Event Type
    Malfunction
    Date Received
    December 6, 2012
    Date of Event
    November 7, 2012
    Report Date
    November 7, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    HDD
    PMA / PMN Number
    K950889
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LIFT MOTOR.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED DRIFTED DOWN WHEN IT WAS RAISED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADEL OBS LABOR AND DELIVERY BED HDD STRYKER MEDICAL 4700 NA

    Patients

    Seq Age Sex Outcome Treatment
    1