BEUDAMED
    FDA Adverse Event Summary report: N

    IN TOUCH ZX

    MDR report key: 1880086 · Received October 19, 2010

    Report

    Report Number
    9680128-2010-00155
    Date Received
    October 19, 2010
    Date of Event
    September 22, 2010
    Report Date
    September 22, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BED HAS INTERMITTENT ZOOM PROBLEMS. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZX HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC LP 2140000000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK