BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    S3 MED/SURG BED

    MDR report key: 1890459 · Received October 27, 2010

    Report

    Report Number
    1831750-2010-03287
    Event Type
    Malfunction
    Date Received
    October 27, 2010
    Date of Event
    September 29, 2010
    Report Date
    September 29, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ORIGINALLY REPORTED BY USER FACILITY THAT THE SCALE WAS NOT FUNCTIONING PROPERLY. UPON ARRIVAL OF THE STRYKER FIELD TECHNICIAN, THE USER FACILITY WAS UNAWARE OF ANY PRODUCT MALFUNCTION. PRODUCT WAS CHECKED AND FOUND TO BE WITHIN SPEC.

    Description of Event or Problem · 1

    IT WAS REPORTED THROUGH A SERVICE REPORT THAT THE SCALE WAS NOT OPERATING PROPERLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 S3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV 3002S3 NA

    Patients

    Seq Age Sex Outcome Treatment
    1