BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZX

    MDR report key: 2190535 · Received November 2, 2007

    Report

    Report Number
    9680128-2007-00008
    Event Type
    Malfunction
    Date Received
    November 2, 2007
    Date of Event
    September 9, 2007
    Report Date
    September 9, 2007
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE UNIT WAS SENT BACK FOR EVALUATION. THE ALLEGED CONDITION COULD NOT BE DUPLICATED.

    Description of Event or Problem · 1

    BED WAS RISING UP WITH PT ON IT UNINTENDEDLY.

    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 2140 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK