BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MD/SUG BED

    MDR report key: 2485240 · Received March 5, 2012

    Report

    Report Number
    1831750-2012-02123
    Event Type
    Malfunction
    Date Received
    March 5, 2012
    Date of Event
    February 6, 2012
    Report Date
    February 6, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: TIMING LINK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE PT HEAD RIGHT SIDE RAIL TIMING LINK WAS BROKEN AND IT COULD NOT BE LOCKED INTO THE UPRIGHT POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MD/SUG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1