BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOOM CRITICAL CARE BED

    MDR report key: 1903314 · Received November 12, 2010

    Report

    Report Number
    1831750-2010-03774
    Event Type
    Malfunction
    Date Received
    November 12, 2010
    Date of Event
    October 18, 2010
    Report Date
    October 18, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: 110V OUTLET. CIRCUIT BREAKER ON BED WAS TRIPPED; THEREFORE, CAUSING THE PRODUCT PLUGGED INTO THE OUTLET TO NOT FUNCTION. PRODUCT PERFORMED AS INTENDED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THERE WAS NO POWER TO THE AUXILIARY POWER OUTLET. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOOM CRITICAL CARE BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 2040 NA

    Patients

    Seq Age Sex Outcome Treatment
    1