BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INVISION-PLUS

    MDR report key: 15008455 · Received July 13, 2022

    Report

    Report Number
    3005951712-2016-00019
    Event Type
    Malfunction
    Date Received
    July 13, 2022
    Date of Event
    March 1, 2016
    Report Date
    July 13, 2022
    Manufacturer
    RYMED TECHNOLOGIES, LLC
    Product Code
    FPA
    PMA / PMN Number
    K991653
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    THIS REPORT IS A POST INSPECTION RETROSPECTIVE REVIEW. 2016 INCIDENT.

    Description of Event or Problem · 0

    ON (B)(6) 2016, THE DISTRIBUTOR REPORTED TO RYMED THAT THEY HAD RECEIVED NOTIFICATION THAT THEIR CUSTOMER HAD EXPERIENCED AN ISSUE WITH THE PRODUCT. REPORTED THAT WHEN THE DEVICE WAS REMOVED FROM THE PACKAGE, THE CAP FELL APART. NO PATIENT INJURY; NEVER REACHED THE PATIENT. 1 SAMPLE WAS RECEIVED ON (B)(6) 2016. IT WAS CONFIRMED THAT THERE WAS 1 INCIDENT WHERE THE CONNECTOR SEPARATED PRIOR TO USE. NO DETAILS SURROUNDING THE INCIDENT ARE AVAILABLE. REPORTED AS PRODUCT CODE 460207, LOT M00153. THIS REPORT IS A POST INSPECTION RETROSPECTIVE REVIEW. 2016 INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    451540 INVISION-PLUS NEEDLELESS IV CONNECTOR FPA RYMED TECHNOLOGIES, LLC M00153

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown