BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 2870625 · Received November 14, 2012

    Report

    Report Number
    1831750-2012-11881
    Event Type
    Malfunction
    Date Received
    November 14, 2012
    Date of Event
    October 16, 2012
    Report Date
    October 16, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LOAD WHEEL, SIDE RAIL.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LOAD WHEEL WAS BROKEN AND THERE WAS A PINCH POINT ON THE SIDE RAIL. THE CUSTOMER REPORTED THAT THEY DID NOT KNOW IF THERE WAS PATIENT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWER PRO AMBULANCE COT WHEELED, STRETCHER FPO STRYKER MEDICAL 6500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1