BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO R4 AMBUL COT

    MDR report key: 2071977 · Received April 19, 2011

    Report

    Report Number
    1831750-2011-03722
    Event Type
    Malfunction
    Date Received
    April 19, 2011
    Date of Event
    March 22, 2011
    Report Date
    March 22, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: LATCH BAR; CHANNEL GUIDE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LATCH BAR IS OVER THE CHANNEL GUIDE. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1