BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZU

    MDR report key: 1982334 · Received January 13, 2011

    Report

    Report Number
    1831750-2011-00494
    Event Type
    Malfunction
    Date Received
    January 13, 2011
    Date of Event
    December 16, 2010
    Report Date
    December 16, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED WILL NOT RAISE OR LOWER ELECTRONICALLY WHEN USING EITHER SIDERAIL OR FOOTBOARD. IT WILL STOP IN MID FUNCTION WHEN YOU TRY TO RAISE OR LOWER THE FOWLER, GATCH, HEIGHT, AND FOOT. ALSO IF YOU TOUCH ANY FUNCTION ON THE FOOTBOARD, THE BED AUTOMATICALLY GOES INTO DRIVE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZU A/C HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 2141 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK