BEUDAMED
    FDA Recall Terminated

    SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray, Product Codes: A119214M, A119216M, A119218M, A119416M, A153200, A300916A, A301216, A301216A, A303314A, A303316A, A303318A, A303414A, A303416A, A303418A, A304400A, A304714A, A304716A, A304718A, A304914, A304916, A304918, A307414A, A307416A, A319414AM, A319416A, A319416AM, A319418AM, A319514AM, A319516A, A319516AM, A333100A, A333416A, A339414AM, A339516AM, A339516AM, A344916, A800064, A800065, A800364, A800365, A800366, A900216, A900416, A901216, A902114, A902216, A902414, A902416, A902418, A902616, A902914, A902916, A902918, A903314A, A903316A, A903318A, A903416A, A904100, A904400A, A909116M, A909216M, A919416AM, A919516AM, A942206, A942208, A942210, A942212, A942214, A942216, A942218, A942616, A942618, A943214, A943216, A943218, MTA902416 Product Usage catheter

    Recall: Z-0803-2019 · Initiated December 13, 2018

    Recall

    Recall Number
    Z-0803-2019
    Event Number
    81889
    Firm
    Bard Medical Division
    FEI Number
    1018233
    Product Code
    MJC
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    December 13, 2018
    Posted
    February 6, 2019
    Terminated
    November 2, 2020
    Address
    8195 Industrial Blvd NE, Covington, GA, 30014-1497

    Description

    SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray, Product Codes: A119214M, A119216M, A119218M, A119416M, A153200, A300916A, A301216, A301216A, A303314A, A303316A, A303318A, A303414A, A303416A, A303418A, A304400A, A304714A, A304716A, A304718A, A304914, A304916, A304918, A307414A, A307416A, A319414AM, A319416A, A319416AM, A319418AM, A319514AM, A319516A, A319516AM, A333100A, A333416A, A339414AM, A339516AM, A339516AM, A344916, A800064, A800065, A800364, A800365, A800366, A900216, A900416, A901216, A902114, A902216, A902414, A902416, A902418, A902616, A902914, A902916, A902918, A903314A, A903316A, A903318A, A903416A, A904100, A904400A, A909116M, A909216M, A919416AM, A919516AM, A942206, A942208, A942210, A942212, A942214, A942216, A942218, A942616, A942618, A943214, A943216, A943218, MTA902416 Product Usage catheter

    Reason

    potential for urine leakage around the vent on the vented sample port

    Action

    Bard sent a Medical Device Notification letter dated December 13, 2018 to affected customers. The letter identified the affected product, problem nd actions to be taken. The distributors were instructed to forward the notice to their affected consignees.

    Distribution

    US, Canada, UAE

    Quantity

    883,171 units