BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 1760428 · Received July 13, 2010

    Report

    Report Number
    1831750-2010-01528
    Event Type
    Injury
    Date Received
    July 13, 2010
    Date of Event
    June 17, 2010
    Report Date
    June 17, 2010
    Manufacturer
    STRYKER CORP MEDICAL DIVISION
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE COT COLLAPSED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R-3 AMBULANCE COT STRECTCHER WHEELED FPO STRYKER CORP MEDICAL DIVISION 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK