BEUDAMED
    FDA Adverse Event Other Summary report: N

    ZOOM CRITICAL CARE BED

    MDR report key: 1982429 · Received January 26, 2011

    Report

    Report Number
    1831750-2011-00813
    Event Type
    Other
    Date Received
    January 26, 2011
    Date of Event
    December 28, 2010
    Report Date
    December 28, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: THE COMPLAINT WAS OF A BURNING SMELL COMING FROM THE BED. THE SERVICE TECHNICIAN COULD NOT DUPLICATE OR VISUALLY FIND ANY PART OF THE BED WHERE SUCH A SMELL COULD BE COMING FROM. THE BED WAS COMPLETELY CHECKED OVER ALL FUNCTIONS WERE CHECKED AND THE SMELL COULD NOT BE REPLICATED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CUSTOMER STATES USERS COMPLAINED OF A BURNING SMELL ALLEGEDLY COMING FROM THE BED. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    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 UNK