BEUDAMED
    FDA Adverse Event Other Summary report: N

    RAPIDCOMM

    MDR report key: 3031922 · Received March 25, 2013

    Report

    Report Number
    1217157-2013-00039
    Event Type
    Other
    Date Received
    March 25, 2013
    Date of Event
    February 26, 2013
    Report Date
    February 27, 2013
    Manufacturer
    SIEMENS HEALTHCARE DIAGNOSTICS
    Product Code
    CHL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE CAUSE FOR THE TRANSFERRING OF INCORRECT INFO IS UNK.

    Description of Event or Problem · 1

    CUSTOMER REPORTS THAT PT INFO WAS CORRECT ON THE RP500 BUT WAS INCORRECT WHEN REPORTED THROUGH RAPIDCOMM ON TWO PT SAMPLES. THERE WAS NO REPORT OF PT INJURY AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    122364 RAPIDCOMM RAPIDCOMM CHL SIEMENS HEALTHCARE DIAGNOSTICS RAPIDC0MM

    Patients

    Seq Age Sex Outcome Treatment
    1