BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IV CONNECT INV PLUS TOUCH

    MDR report key: 20474178 · Received October 16, 2024

    Report

    Report Number
    MW5161161
    Event Type
    Injury
    Date Received
    October 16, 2024
    Date of Event
    September 7, 2024
    Report Date
    September 7, 2024
    Manufacturer
    RYMED TECHNOLOGIES, LLC
    Product Code
    FPA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT CALLED AND INFORMED THAT HER IV CONNECT INV PLUS TOUCH WAS NOT WORKING AND THAT SHE REPLACED IT. THE PUMP NOW WORKS FINE AND SHE FEELS LIKE THE PUMP IS DELIVERING THE RIGHT AMOUNT OF MEDICATION. NO ADDITIONAL INFORMATION OR DETAILS AVAILABLE. REPORTED TO (B)(6) BY: PATIENT/CAREGIVER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2270920 IV CONNECT INV PLUS TOUCH SET, ADMINISTRATION, INTRAVASCULAR FPA RYMED TECHNOLOGIES, LLC RYM-5000

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Female