BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    S3 EX- 3005

    MDR report key: 2873530 · Received November 15, 2012

    Report

    Report Number
    1831750-2012-11991
    Event Type
    Malfunction
    Date Received
    November 15, 2012
    Date of Event
    October 23, 2012
    Report Date
    October 23, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ISSUE WAS RESOLVED FOR THE CUSTOMER BY THE SERVICE TECH REINSTALLING THE WIRE ON THE MOTION INTERRUPT SWITCH. AFTER RE-CONNECTING WIRE, THE SERVICE TECH CHECKED THAT THE MOTION INTERRUPT PAN WAS WORKING PROPERLY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED LIFT WAS STUCK IN AN ELEVATED POSITION DUE TO A MOTION INTERRUPT SWITCH WIRE COMING LOOSE FROM THE CPU. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 S3 EX- 3005 A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3005S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1