BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO R4 AMBUL COT

    MDR report key: 2861826 · Received November 8, 2012

    Report

    Report Number
    1831750-2012-11692
    Event Type
    Malfunction
    Date Received
    November 8, 2012
    Date of Event
    October 12, 2012
    Report Date
    October 12, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEIGHT ADJUSTMENT FUNCTION OF THE COT WAS NO LONGER FUNCTIONAL DUE TO A DAMAGED LOCK PIN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZ-PRO R4 AMBUL COT WHEELED, STRETCHER FPO STRYKER MEDICAL 6092 NA

    Patients

    Seq Age Sex Outcome Treatment
    1