BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IN TOUCH ZU

    MDR report key: 2967744 · Received February 19, 2013

    Report

    Report Number
    0001831750-2013-01291
    Event Type
    Injury
    Date Received
    February 19, 2013
    Date of Event
    January 24, 2013
    Report Date
    January 24, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS REPORTED BED EXIT SYSTEM WAS NOT SET.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COMPLAINANT ALLEGED BED ALARM DID NOT SOUND ON INTOUCH BED, CAUSING ALLEGED PATIENT FALL AND INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    71120 IN TOUCH ZU BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1