BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GERMSTAR PAIN MGE SNG

    MDR report key: 3832187 · Received March 7, 2014

    Report

    Report Number
    9615050-2014-01758
    Event Type
    Malfunction
    Date Received
    March 7, 2014
    Date of Event
    January 14, 2014
    Report Date
    January 17, 2014
    Manufacturer
    HOSPIRA COSTA RICA LTD.
    Product Code
    FRN
    PMA / PMN Number
    K060806
    Removal / Correction Number
    Z-1159-2013
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DURING TESTING, AT POWER UP THE DEVICE ALARMED FOR 18/00/000 (HISTORY POINTER ERROR) AND 11/004 (LESS THAN 2.0 VOLTS ON LITHIUM BATTERY) SERVICE ALARM CODE. THE DEVICE HAS BEEN IDENTIFIED AS PART OF A PRODUCT RECALL. THIS REPORT REPRESENTS ALL THE INFORMATION KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL

    Description of Event or Problem · 1

    THE DEVICE WAS RETURNED TO THE SERVICE CENTER WITH A REPORT FROM THE CUSTOMER CONTACT THAT DURING ROUTINE TESTING AT THE USER FACILITY THE DEVICE ALARMED WITH A 18/000/000 (HISTORY POINTER ERROR) SERVICE ALARM CODE. THIS IS NOT A REPORTABLE MALFUNCTION. HOWEVER, DURING VERIFICATION TESTING AT THE SERVICE CENTER THE DEVICE ALARMED WITH A 11/004 (LESS THAN 2.0 VOLTS ON LITHIUM BATTERY).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    138534 GERMSTAR PAIN MGE SNG 80FRN FRN HOSPIRA COSTA RICA LTD. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA