BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 BED/SURG BED

    MDR report key: 1890453 · Received October 27, 2010

    Report

    Report Number
    1831750-2010-03295
    Event Type
    Malfunction
    Date Received
    October 27, 2010
    Date of Event
    September 28, 2010
    Report Date
    September 28, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    I-BED SYSTEM. MANUFACTURERS INVESTIGATION IS STILL ONGOING. IF ANY ADDITIONAL INFO IS RECEIVED, A F/U WILL BE ISSUED.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE IBED AWARENESS LIGHTS ARE NOT WORKING. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 BED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 3002S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1