BEUDAMED
    FDA Adverse Event Other Summary report: N

    SM204 M-SERIES W/BIG WHEEL

    MDR report key: 1003062 · Received February 22, 2008

    Report

    Report Number
    1831750-2008-00017
    Event Type
    Other
    Date Received
    February 22, 2008
    Date of Event
    January 25, 2008
    Report Date
    January 25, 2008
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE BRAKES DO NOT APPLY SUFFICIENT PRESSURE TO HOLD THE STRETCHER IN PLACE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM204 M-SERIES W/BIG WHEEL STRETCHER FPO STRYKER CORP., MEDICAL DIVISION 1015 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention