BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3002 SECURE II MED/SURG BED

    MDR report key: 2914262 · Received December 6, 2012

    Report

    Report Number
    1831750-2012-12295
    Event Type
    Malfunction
    Date Received
    December 6, 2012
    Date of Event
    November 1, 2012
    Report Date
    November 1, 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: BROKEN TIMING LINK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD RIGHT SIDE RAIL ASSEMBLY TIMING LINK WAS BROKEN AND DIDN'T ALLOW THE SIDE RAIL TO LOCK. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 3002 SECURE II MED/SURG BED AC POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1