BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OB-GYN STRETCHER OBS 9/00

    MDR report key: 2942727 · Received February 4, 2013

    Report

    Report Number
    0001831750-2013-00704
    Event Type
    Malfunction
    Date Received
    February 4, 2013
    Date of Event
    January 11, 2013
    Report Date
    January 11, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: BRAKE CAM.

    Additional Manufacturer Narrative · 1

    RESULT: BRAKE ADJUSTER.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE FOOT END BRAKE DOES NOT HOLD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE FOOT END BRAKE DOES NOT HOLD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    47279 OB-GYN STRETCHER OBS 9/00 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1