BEUDAMED
    FDA Recall Terminated

    Tri-Plex Adapter, single unit (MD-04000 )or box of 25 (MD-04001) or case of 100 (MD-04002). Sterile. Single Use.

    Recall: Z-1371-05 · Initiated June 8, 2005

    Recall

    Recall Number
    Z-1371-05
    Event Number
    32468
    Firm
    Medical Device Group Inc.
    FEI Number
    3004500043
    Product Code
    MOD
    Status
    Terminated
    Root Cause
    Other
    Initiated
    June 8, 2005
    Posted
    August 16, 2005
    Terminated
    April 6, 2012
    Address
    12675 Stowe Dr, Ste B, Poway, CA, 92064-8848

    Description

    Tri-Plex Adapter, single unit (MD-04000 )or box of 25 (MD-04001) or case of 100 (MD-04002). Sterile. Single Use.

    Reason

    Device separation presenting a choking hazard.

    Action

    Distributors were contacted by telephone on June 8, 2005, distributors were requested to return product. Letters were also sent by mail with proof of reciept on June 10, 2005. Firm reports that all customers have been notified.

    Distribution

    Nationwide, Brasil and Canada

    Quantity

    2,282