BEUDAMED
    FDA Recall Terminated

    Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and MV-AZ52030HD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

    Recall: Z-1223-2020 · Initiated November 24, 2019

    Recall

    Recall Number
    Z-1223-2020
    Event Number
    84585
    Firm
    Microvention, Inc.
    FEI Number
    3003523199
    Product Code
    KRD
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 24, 2019
    Terminated
    April 20, 2021
    Address
    35 Enterprise, Aliso Viejo, CA, 92656-2601

    Description

    Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and MV-AZ52030HD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

    Reason

    The devices may be missing the implant coil.

    Action

    The recalling firm issued emails dated 11/24/2019 to the Terumo distributors and provided instructions for notification of their customers (physicians).

    Distribution

    The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.

    Quantity

    392 units