BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GYNNIE OB-GYN STRETCHER

    MDR report key: 2920425 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12578
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 7, 2012
    Report Date
    November 7, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    PUMP PEDAL ASSEMBLY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE JACKS COULD NOT BE PUMPED UP DUE TO A BROKEN PUMP PEDAL ASSEMBLY. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1