BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZU

    MDR report key: 2864630 · Received November 9, 2012

    Report

    Report Number
    1831750-2012-11729
    Event Type
    Malfunction
    Date Received
    November 9, 2012
    Date of Event
    October 25, 2012
    Report Date
    October 25, 2012
    Manufacturer
    FLEXTRONICS EMS CANADA
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: TRIPPED BREAKER, CONCLUSION: BREAKER RESET AND BED RETURNED TO SERVICE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS NO POWER TO THE AUXILIARY OUTLET. THE CUSTOMER REPORTED THAT THEY DID NOT KNOW IF THERE WAS PATIENT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZU A/C HOSPITAL BED FNL FLEXTRONICS EMS CANADA 2141 NA

    Patients

    Seq Age Sex Outcome Treatment
    1