BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PACU DESIGNER MOD.

    MDR report key: 1898848 · Received November 8, 2010

    Report

    Report Number
    1831750-2010-03583
    Event Type
    Malfunction
    Date Received
    November 8, 2010
    Date of Event
    October 12, 2010
    Report Date
    October 12, 2010
    Manufacturer
    STRYKER CORP, MED DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER KEEPS DRIFTING DOWN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PACU DESIGNER MOD. HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MED DIV 0946

    Patients

    Seq Age Sex Outcome Treatment
    1 NA