BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO 2 AMBUL COT

    MDR report key: 1894683 · Received November 5, 2010

    Report

    Report Number
    1831750-2010-03543
    Event Type
    Malfunction
    Date Received
    November 5, 2010
    Date of Event
    October 12, 2010
    Report Date
    October 12, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE UNIT WAS NOT LOCKING PROPERLY. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZ-PRO 2 AMBUL COT STRETCHER, WHEELED FPO STRYKER CORP., MEDICAL DIVISION 6091 NA

    Patients

    Seq Age Sex Outcome Treatment
    1