BEUDAMED
    FDA Enforcement Class II Ongoing

    DuraLife Autoclavable Silicone Extension Tube, REF 60-1502 (UltraSet Product Code 66-2509); Non-Ported Double Swivel Elbow for use with breathing circuits

    Recall: Z-1581-2023 · Reported May 24, 2023

    Enforcement

    Recall Number
    Z-1581-2023
    Event ID
    91975
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Smiths Medical ASD Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    May 24, 2023
    Initiation Date
    April 5, 2023
    Classification Date
    May 12, 2023
    Address
    6000 Nathan Ln N, N/A, Minneapolis, MN, 55442-1690, United States

    Description

    DuraLife Autoclavable Silicone Extension Tube, REF 60-1502 (UltraSet Product Code 66-2509); Non-Ported Double Swivel Elbow for use with breathing circuits

    Reason

    DuraLife devices instructions for cleaning and sterilization have been determined to be inadequate. Specifically, for the DuraLife product, the IFU does not provide the cleaning method, duration of autoclave cycle or specify the number of cycles the product can be reused on a single patient.

    Code Info

    3569291, 3802463, 3974741, 4093611, 4219069, 4340640, 3582651, 3832622, 4001787, 4108514, 4242510, 4340642, 3609721, 3871182, 4011956, 4116120, 4254340, 3609743, 3891814, 4032896, 4122394, 4264898, 3693349, 3914797, 4041943, 4151071, 4279831, 3723464, 3927549, 4063256, 4167796, 4290272, 3761125, 3952707, 4090324, 4182390, 4340638

    Distribution

    Worldwide distribution - US Nationwide and the countries of Canada, New Zealand, and Hong Kong.

    Quantity

    2101 units