BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 1974090 · Received December 28, 2010

    Report

    Report Number
    1831750-2010-05246
    Event Type
    Malfunction
    Date Received
    December 28, 2010
    Date of Event
    November 30, 2010
    Report Date
    November 30, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOTBOARD CONNECTOR CRACKED CAUSING FOOTBOARD CONTROLS NOT TO WORK AND THE SIDERAIL CONTROLS WERE NOT WORKING. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 3002S3 NA

    Patients

    Seq Age Sex Outcome Treatment
    1