BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTAGE SERIES 26

    MDR report key: 1893754 · Received November 2, 2010

    Report

    Report Number
    1831750-2010-03491
    Event Type
    Malfunction
    Date Received
    November 2, 2010
    Date of Event
    October 12, 2010
    Report Date
    October 12, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THROUGH A SERVICE REPORT THAT THE FOWLER WAS NOT LOWERING ALL THE WAY. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTAGE SERIES 26 HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1001 NA

    Patients

    Seq Age Sex Outcome Treatment
    1