BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 29

    MDR report key: 2914876 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12631
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 8, 2012
    Report Date
    November 8, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL COULD NOT REMAIN LATCHED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAISSANCE 29 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1710 NA

    Patients

    Seq Age Sex Outcome Treatment
    1