BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 1191388 · Received September 26, 2008

    Report

    Report Number
    1831750-2008-00132
    Event Type
    Malfunction
    Date Received
    September 26, 2008
    Date of Event
    August 20, 2008
    Report Date
    August 29, 2008
    Manufacturer
    STRYKER CORP . MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    GIVEN CURRENT INFO, IT IS LIKELY THAT REPETITIVE LOADS ABOVE SPECIFICATIONS MAY HAVE CONTRIBUTED TO THE EVENT. THE DEVICE IS ENROUTE FOR EVALUATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE LOAD WHEEL CASTING BROKE. NO INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWER PRO AMBULANCE COT AMBULANCE COT FPO STRYKER CORP . MEDICAL

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK