BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 2022494 · Received February 15, 2011

    Report

    Report Number
    1831750-2011-01396
    Event Type
    Malfunction
    Date Received
    February 15, 2011
    Date of Event
    January 14, 2011
    Report Date
    January 17, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A FEMALE PT SUFFERED FROM A CONTUSION WHEN THE COT TIPPED. NO MEDICAL INTERVENTION WAS REQUIRED. THE COT WAS INSPECTED AND IT WAS DETERMINED THAT THE COT WAS NOT AT FAULT AND WAS OPERATING TO SPECIFICATION. THERE WAS A MISCOMMUNICATION AS THE TWO MEDICS WERE PULLING THE COT OUT OF THE AMBULANCE. ONE MEDIC RELEASED THE SAFETY BAR PRIOR TO THE WHEELS BEING LOWERED. PT INVOLVEMENT HAS BEEN REPORTED, HOWEVER, NO ADVERSE CONSEQUENCES TO REPORT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR