BEUDAMED
    FDA Recall Terminated

    Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK.

    Recall: Z-0808-2013 · Initiated August 21, 2012

    Recall

    Recall Number
    Z-0808-2013
    Event Number
    63556
    Firm
    Remel Inc
    FEI Number
    1924669
    Product Code
    JTN
    Status
    Terminated
    Root Cause
    Nonconforming Material/Component
    Initiated
    August 21, 2012
    Posted
    February 12, 2013
    Terminated
    June 4, 2013
    Address
    12076 Santa Fe Trail Dr, Lenexa, KS, 66215-3519

    Description

    Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK.

    Reason

    The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.

    Action

    The recalling firm sent a recall notification letter dated 8/17/ 2012 and 8/21/2012.

    Distribution

    US Nationwide Distribution including the states of: CA, CT, GA, IA, KS, OK, RI, TX, WA, WI,

    Quantity

    23 units