BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CS300

    MDR report key: 2862152 · Received November 29, 2012

    Report

    Report Number
    2249723-2012-00445
    Event Type
    Malfunction
    Date Received
    November 29, 2012
    Date of Event
    October 12, 2012
    Report Date
    October 12, 2012
    Manufacturer
    DATASCOPE CORP.
    Product Code
    DSP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE COMPANY REPRESENTATIVE CONFIRMED THE FAILURE CODE IN THE FAULT LOG, ALONG WITH "LOW VACUUM" AND "SYSTEM FAILURE" ALARMS. HE REPLACED THE DRIVE TRANSDUCER (PART NUMBER (B)(4)). THE IABP WAS TESTED TO FACTORY SPECIFICATION. IT FUNCTIONED NORMALLY AND WAS RETURNED TO THE CUSTOMER.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT WHILE THE IABP WAS IN USE ON A PATIENT, THE IABP GENERATED "ELECTRICAL TEST FAILURE CODE # 53" (SHUTTLE TRANSDUCER OFFSET FAILURE) AND THEN STOPPED. THE CUSTOMER REBOOTED THE IABP AND THERAPY WAS CONTINUED. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CS300 INTRA-AORTIC BALLOON PUMP DSP DATASCOPE CORP. CS300

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK