BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GYNNIE OB-GYN STRETCHER

    MDR report key: 2133184 · Received May 4, 2011

    Report

    Report Number
    1831750-2011-04321
    Event Type
    Malfunction
    Date Received
    May 4, 2011
    Date of Event
    April 6, 2011
    Report Date
    April 6, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    HDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD OF THE STRETCHER WOULD NOT PUMP UP. NO PATIENT 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 NA