BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SM 104 M-SERIES W/5TH WHL

    MDR report key: 1506861 · Received September 25, 2009

    Report

    Report Number
    1831750-2009-01292
    Event Type
    Malfunction
    Date Received
    September 25, 2009
    Date of Event
    August 5, 2009
    Report Date
    August 27, 2009
    Manufacturer
    STRYKER CORP, MEDICAL STRETCHER
    Product Code
    FPO
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SZ
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NA

    Description of Event or Problem · 1

    IT WAS REPORTED, THE BRAKES WERE NOT FUNCTIONING TO SPECIFICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM 104 M-SERIES W/5TH WHL HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL STRETCHER 1007 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA