BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZU

    MDR report key: 2962312 · Received February 14, 2013

    Report

    Report Number
    0001831750-2013-01183
    Event Type
    Malfunction
    Date Received
    February 14, 2013
    Date of Event
    January 18, 2013
    Report Date
    January 18, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): ONCE THE PRODUCT HAS BEEN EVALUATED A SUPPLEMENTAL REPORT WILL BE FILED, IF APPROPRIATE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE GROUND PATH WAS COMPROMISED WHEN THE BED WAS PLUGGED IN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    65922 IN TOUCH ZU BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1