BEUDAMED
    FDA Recall Terminated

    Terumo Perfusion System 8000 Roller Pump, 220/240V; Model 8000; Catalog No. 16407.

    Recall: Z-1003-2007 · Initiated July 1, 2004

    Recall

    Recall Number
    Z-1003-2007
    Event Number
    37367
    Firm
    Terumo Cardiovascular Systems Corp
    FEI Number
    1828100
    Product Code
    DTQ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    July 1, 2004
    Posted
    July 7, 2007
    Terminated
    December 12, 2007
    Address
    6200 Jackson Rd, Ann Arbor, MI, 48103-9586

    Description

    Terumo Perfusion System 8000 Roller Pump, 220/240V; Model 8000; Catalog No. 16407.

    Reason

    Roller Pump: Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

    Action

    As the complaints were received (between 07/04 and 01/06), the firm visited the customer filing the complaint and repaired the pumps demonstrating the problem. The firm will correct other units as complaints are received. The firm modified its recall strategy and issued a Device Correction Letter dated 6/22/07 notifying all users of the problem

    Distribution

    Worldwide: USA and Bangladesh, Belgium, Bolivia, Canada, Chile, Colombia, Costa Rica, Egypt, Equador, Hong Kong, India, Indonesia, Japan, Latin America, Malaysia, Nicaragua, Philippines, Saudi Arabia, Taipe, Taiwan, United Arab Emirates, Uruguay, and Viet Nam.

    Quantity

    728 pumps of all models