BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO R4 AMBUL COT

    MDR report key: 1890501 · Received October 27, 2010

    Report

    Report Number
    1831750-2010-03325
    Event Type
    Malfunction
    Date Received
    October 27, 2010
    Date of Event
    October 1, 2010
    Report Date
    October 1, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    ROLLER.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE RELEASE MECHANISM WAS NOT FUNCTIONING PROPERLY. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1