BEUDAMED
    FDA Enforcement Class II Terminated

    Duo-Flow Catheter Full Tray; MCDLT3500 MCDLT4000 MCDLT4400 MCDLT4424# Hemodialysis catheter insertion kits

    Recall: Z-2936-2018 · Reported September 5, 2018

    Enforcement

    Recall Number
    Z-2936-2018
    Event ID
    80581
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Medical Components, Inc dba MedComp
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    September 5, 2018
    Initiation Date
    July 12, 2018
    Classification Date
    August 25, 2018
    Termination Date
    July 2, 2020
    Address
    1499 Delp Dr, N/A, Harleysville, PA, 19438-2936, United States

    Description

    Duo-Flow Catheter Full Tray; MCDLT3500 MCDLT4000 MCDLT4400 MCDLT4424# Hemodialysis catheter insertion kits

    Reason

    The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious injury or death.

    Code Info

    MKAZ210 MCBK870 MCBS910 MCBZ450 MCCP990 MCCZ440 MCDNlOO MCDQ930 MCFD710 MCFN970 MCFS730 MCAS340 MCBA830 MCBR880 MCBY910 MCCF130 MCCX150 MCDF010 MCDG980 MCDP120 MCFD720 MCFJ060 MCFM520 MCFW300 MCFZ590 MKAJ380 MCAS230 MCBL150 MCBN500 MCBZ380 MCCV010 MCDF030 MCFX080 MCFV620 MCBA170 MCDC940 MKAX240 MCAC870 MCCQ000 MCFG380 MKAQ920 MCAH920 MCCW950

    Distribution

    Nationwide distribution; worldwide distribution.

    Quantity

    N/A