BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZX

    MDR report key: 2023959 · Received February 14, 2011

    Report

    Report Number
    1831750-2011-01383
    Event Type
    Malfunction
    Date Received
    February 14, 2011
    Date of Event
    November 10, 2010
    Report Date
    November 10, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD END WILL NOT CALIBRATE. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZX A/C HOSPITAL BED FNL STRYKER MEDICAL 2140 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK