BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO 2 AMBUL COT

    MDR report key: 2000311 · Received February 18, 2011

    Report

    Report Number
    1831750-2011-01606
    Event Type
    Malfunction
    Date Received
    February 18, 2011
    Date of Event
    January 20, 2011
    Report Date
    January 20, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT SIDE WHEELS ARE ALLEGEDLY BENT. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1