BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GYNNIE OB-GYN STRETCHER

    MDR report key: 2141366 · Received June 1, 2011

    Report

    Report Number
    1831750-2011-05358
    Event Type
    Malfunction
    Date Received
    June 1, 2011
    Date of Event
    May 4, 2011
    Report Date
    May 4, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    HDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL RESULT: RELEASE ROD AND RELEASE PADDLE. CONCLUSION: THE PUSH RELEASE ROD AND THE RELEASE PADDLE WERE STUCK DUE TO DUST/DIRT WHICH KEPT THE RELIEF VALVE ASSEMBLY OPEN AND PREVENTED THE FOOT END JACK FROM PUMPING UP.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE FOOT END OF THE STRETCHER WOULD NOT PUMP UP. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GYNNIE OB-GYN STRETCHER HOSPITAL WHEELED STRETCHER HDD STRYKER MEDICAL 1061 NA

    Patients

    Seq Age Sex Outcome Treatment
    1