BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANIMAS INSULIN INFUSION PUMP

    MDR report key: 2451420 · Received February 14, 2012

    Report

    Report Number
    2531779-2012-01150
    Event Type
    Malfunction
    Date Received
    February 14, 2012
    Report Date
    November 7, 2011
    Manufacturer
    ANIMAS CORPORATION
    Product Code
    LZG
    PMA / PMN Number
    K042873
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    THE PUMP HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON 01/18/2012 WITH THE FOLLOWING FINDINGS: DURING INVESTIGATION, EVIDENCE OF LOSS OF PRIME WAS FOUND IN THE PUMP HISTORY BUT COULD NOT BE DUPLICATED DURING TESTING. EVALUATION REVEALED THAT THE FORCE SENSOR WAS DETECTING CORRECT FORCE AND WAS OPERATING WITHIN SPECIFICATION. IT WAS DISCOVERED THAT THE FORCE SENSOR FLEX PINS WERE PARTIALLY SEATED IN THE FORCE SENSOR SOCKET. ANIMAS HAS CONDUCTED A REVIEW OF THE DEVICE HISTORY RECORD FOR THIS PUMP AND CONFIRMED THAT IT WAS OPERATING WITHIN REQUIRED SPECIFICATIONS AT THE TIME OF RELEASE. CORRECTION NUMBER: 2531779-03/24/2010-003-R

    Description of Event or Problem · 1

    THE PUMP WAS RETURNED FOR INVESTIGATION AND EVALUATION REVEALED A FORCE SENSOR DEFECT THAT HAD NOT BEEN REPORTED BY THE USER. THIS REPORT IS MADE BASED ON RESULTS OF INVESTIGATION COMPLETED ON 01/18/2012.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ANIMAS INSULIN INFUSION PUMP INSULIN INFUSION PUMP LZG ANIMAS CORPORATION ANM 2020 INSULIN INFUSION PUMP

    Patients

    Seq Age Sex Outcome Treatment
    1