BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 2873727 · Received November 14, 2012

    Report

    Report Number
    1831750-2012-11856
    Event Type
    Malfunction
    Date Received
    November 14, 2012
    Date of Event
    October 19, 2012
    Report Date
    October 19, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: FOOT COVER ASSEMBLY. LIFT POWER COIL CABLE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END LIFT WAS STUCK IN AN ELEVATED POSITION DUE TO LIFT POWER COIL CABLE BEING OUT, RESULTING IN EXPOSED WIRING CARRYING 110 VOLTS AC, AND THE FOOT COVER ASSEMBLY WAS BENT, PRESENTING SHARP EDGES. 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 FPO STRYKER MEDICAL 3002S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1