BEUDAMED
    FDA Enforcement Class II Terminated

    191 cm (75") Appx 2.9 ml, PVC/PUR Smallbore Bifuse Ext Set w/6-Port NanoClave Manifold w/2 Red Rings, Check Valve, 2 MicroClave Clear, Clamp, Rotating Luer.

    Recall: Z-2807-2018 · Reported August 22, 2018

    Enforcement

    Recall Number
    Z-2807-2018
    Event ID
    80460
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    ICU Medical de Mexico, S.A. de C.V.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    August 22, 2018
    Initiation Date
    March 1, 2018
    Classification Date
    August 16, 2018
    Termination Date
    January 26, 2024
    Address
    Avenida Cuarzo 250, Ensenada, Ejido Maneadero, N/A, Mexico

    Description

    191 cm (75") Appx 2.9 ml, PVC/PUR Smallbore Bifuse Ext Set w/6-Port NanoClave Manifold w/2 Red Rings, Check Valve, 2 MicroClave Clear, Clamp, Rotating Luer.

    Reason

    ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.

    Code Info

    Item Number 011-AM6125. Lot Number 3424313, UDI Number (01) 1 0840619 09486 4 (17) 220301 (30) 50 (10) 342313, Expiration Date 03/01/2022

    Distribution

    US distribution to AZ, MA, NC, OH, TX, VA, WA. Worldwide distribution to Belgium, France, Germany.

    Quantity

    50 pouches