BEUDAMED
    FDA Recall Terminated

    Flexiflo Quantum Enteral Pump

    Recall: Z-0570-05 · Initiated August 18, 2004

    Recall

    Recall Number
    Z-0570-05
    Event Number
    29856
    Firm
    Ross Products Division Abbott Laboratories
    FEI Number
    1000136098
    Product Code
    LZH
    Status
    Terminated
    Root Cause
    Other
    Initiated
    August 18, 2004
    Posted
    March 8, 2005
    Terminated
    April 12, 2012
    Address
    625 Cleveland Ave, Columbus, OH, 43215-1754

    Description

    Flexiflo Quantum Enteral Pump

    Reason

    Pumps were manufactured with an incorrect circuit board that may cause an increase in the feed rate and flush frequency of fluids.

    Action

    The firm contacted all consignees via telephone and letter on 08/18/2004.

    Distribution

    Products were distributed to the following states nationwide: MA, NJ, NY, PA, MD, VA, NC, SC, GA, FL, CA, TN, KY, OH, MI, SD, IL, KS, LA, AR, OK, TX, and CO.

    Quantity

    199 individual serial numbered units