BEUDAMED
    FDA Enforcement Class I Ongoing

    Baxter Spectrum IQ Infusion Pumps, Product code 3570009.

    Recall: Z-0529-2022 · Reported February 9, 2022

    Enforcement

    Recall Number
    Z-0529-2022
    Event ID
    89017
    Classification
    Class I
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Baxter Healthcare Corporation
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    February 9, 2022
    Initiation Date
    December 29, 2021
    Classification Date
    January 28, 2022
    Address
    1 Baxter Pkwy, N/A, Deerfield, IL, 60015-4625, United States

    Description

    Baxter Spectrum IQ Infusion Pumps, Product code 3570009.

    Reason

    There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms when using Spectrum V8 and Spectrum IQ infusion pumps.

    Code Info

    All serial numbers, GTIN 00085412610900.

    Distribution

    Worldwide Distribution. US nationwide Puerto Rico and St. Thomas. There was government/military distribution. Countries of Canada, Bahamas, Barbados, Bermuda, Guyana, Jamaica, and Trinidad and Tobago.

    Quantity

    241,304 units