BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO R4 AMBUL COT

    MDR report key: 2091236 · Received April 20, 2011

    Report

    Report Number
    1831750-2011-03845
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Date of Event
    March 25, 2011
    Report Date
    March 25, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LATCH LEVER.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT TWO SPRINGS WERE MISSING AND THE LATCH LEVER IS DAMAGED. 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 STETCHER, WHEELED INK STRYKER MEDICAL 6092 NA

    Patients

    Seq Age Sex Outcome Treatment
    1