BEUDAMED
    FDA Enforcement Class II Terminated

    ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial Catalog Number: M57230600220 (US) M5723INT0600220 (OUS)

    Recall: Z-0143-2016 · Reported October 28, 2015

    Enforcement

    Recall Number
    Z-0143-2016
    Event ID
    72108
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    ConforMIS, Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
    Report Date
    October 28, 2015
    Initiation Date
    August 31, 2015
    Classification Date
    October 21, 2015
    Termination Date
    March 2, 2016
    Address
    28 Crosby Dr, N/A, Bedford, MA, 01730-1402, United States

    Description

    ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial Catalog Number: M57230600220 (US) M5723INT0600220 (OUS)

    Reason

    May contain small amounts of ethylene glycol residue

    Code Info

    Serial Numbers (US): 0354902, 0353696 Serial Numbers (OUS): 0349179 0352344 0352431 0352626 0353845 0353883 0353884 0354625 0355002 0355181

    Distribution

    Distributed Nationwide and in Germany, Switzerland, and UK.

    Quantity

    12 units