BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CS100

    MDR report key: 2072818 · Received March 31, 2011

    Report

    Report Number
    2249723-2011-00009
    Event Type
    Malfunction
    Date Received
    March 31, 2011
    Date of Event
    January 5, 2011
    Report Date
    January 5, 2011
    Manufacturer
    DATASCOPE CORP.
    Product Code
    DSP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE COMPANY REP WAS UNABLE TO DUPLICATE THE REPORTED PROBLEM. AS A PRECAUTIONARY MEASURE, THE BATTERIES ((B)(4)) WERE REPLACED. THE UNIT WAS TESTED TO FACTORY SPECIFICATION. IT FUNCTIONED NORMALLY AND WAS RETURNED TO THE CUSTOMER. THE REPORTED FAILURE COULD NOT BE REPRODUCED. A REVIEW OF THE IABP'S SERVICE HISTORY DOES NOT INDICATE ANY SYSTEMIC ISSUES.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT DURING TRANSPORTATION IN AN AMBULANCE, WHILE THE UNIT WAS IN USE ON A PT, THE UNIT SHUTDOWN ON BATTERIES WITH INDICATOR ON SCREEN AT 3/4. WHEN THE UNIT WAS PLUGGED IN, THE AMBULANCE CIRCUIT BREAKER TRIPPED. THE PT WAS SWITCHED TO ANOTHER UNIT AND THERAPY WAS CONTINUED. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CS100 INTRA-AORTIC BALLOON PUMP DSP DATASCOPE CORP. CS100

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK