BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    S3 EX - 3005

    MDR report key: 2873651 · Received November 14, 2012

    Report

    Report Number
    1831750-2012-11790
    Event Type
    Malfunction
    Date Received
    November 14, 2012
    Date of Event
    October 16, 2012
    Report Date
    October 16, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: DIP SWITCHES ON THE CPU BOARDS WERE CONFIGURED INCORRECTLY. CONCLUSION: DIP SWITCHES RECONFIGURED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE NURSE CALL WAS NOT WORKING. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 S3 EX - 3005 A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3005S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1