BEUDAMED
    FDA Adverse Event Other Summary report: N

    SM104 M-SERIES W/5TH WHEEL

    MDR report key: 1032474 · Received April 18, 2008

    Report

    Report Number
    1831750-2008-00074
    Event Type
    Other
    Date Received
    April 18, 2008
    Date of Event
    March 18, 2008
    Report Date
    March 19, 2008
    Manufacturer
    STRYKER CORP, MEDICAL DIV
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE BRAKES WERE NOT WORKING PROPERLY ON THIS STRETCHER. THERE WAS NO PATIENT OR USER INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM104 M-SERIES W/5TH WHEEL STRETCHER FPO STRYKER CORP, MEDICAL DIV 1007 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention