BEUDAMED
    FDA Enforcement Class II Terminated

    Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery.

    Recall: Z-0158-2015 · Reported November 12, 2014

    Enforcement

    Recall Number
    Z-0158-2015
    Event ID
    58185
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Terumo Cardiovascular Systems Corp
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    November 12, 2014
    Initiation Date
    March 1, 2011
    Classification Date
    October 31, 2014
    Termination Date
    November 6, 2014
    Address
    28 Howe St, N/A, Ashland, MA, 01721-1305, United States

    Description

    Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery.

    Reason

    Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

    Code Info

    Lot Numbers: MN08, MNI5, MM11, MM18, MM25. Manufacturing dates October 1I, 2010 through Novemberl5, 20 I 0.

    Distribution

    Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

    Quantity

    777 units