BEUDAMED
    FDA Adverse Event Other Summary report: N

    EZ-PRO 2 AMBUL COT

    MDR report key: 2010409 · Received March 1, 2011

    Report

    Report Number
    1831750-2011-02018
    Event Type
    Other
    Date Received
    March 1, 2011
    Date of Event
    January 28, 2011
    Report Date
    January 31, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THERE WAS AN INCIDENT INVOLVING A STRETCHER AND A PT. ACCORDING TO THE SALES REP, THE EMPLOYEE WAS INJURED AND EXPERIENCED BACK PAIN. THERE WAS REPORTED PT INVOLVEMENT AND ADVERSE CONSEQUENCES.

    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