BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLUOROSCOPY STRETCHER

    MDR report key: 2021511 · Received February 16, 2011

    Report

    Report Number
    1831750-2011-01485
    Event Type
    Malfunction
    Date Received
    February 16, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE HYDRAULICS HAVE FAILED ON THE STRETCHER. WHEN THE LEVER WAS PULLED, THIS WOULD ONLY RAISE THE HEAD END BUT NOT THE FOOT END OF THE STRETCHER. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLUOROSCOPY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA