BEUDAMED
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    Biomet CC Cruciate Tibial Tray, 67 mm.; Product No. 141232, Biomet, Inc., Warsaw, IN 46581

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·December 12, 2007

    Biomet CC Cruciate Tibial Tray, 75 mm.; Product No. 141234, Biomet, Inc., Warsaw, IN 46581

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·December 12, 2007

    Biomet Optigun Cement Gun, non-sterile; REF 419300 and REF 4193 (in Europe), Biomet, Inc., Warsaw, IN

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·September 21, 2007

    Biomet Optigun Cement Gun, Ratchet, non-sterile; REF 419500 and REF 4195 (in Europe), Biomet, Inc., Warsaw, IN

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·September 21, 2007

    Biomet RINGLOC + Instrumentation Impactor Plate, Size 21; REF 31-400621,Biomet Orthopedics, Inc., Warsaw, IN.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·October 18, 2007

    Biomet RINGLOC + Instrumentation Impactor Plate, Size 28; REF/Part#: 31-400628, Biomet Orthopedics, Inc., Warsaw, IN.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·October 18, 2007

    Biomet RINGLOC + Instrumentation Impactor Plate, Size 20; REF/Part #: 31-400620, Biomet Orthopedics, Inc., Warsaw, IN.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·October 18, 2007

    Biomet RINGLOC + Instrumentation Impactor Plate, Size 26; REF/Part#: 31-400626, Biomet Orthopedics, Inc., Warsaw, IN.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·October 18, 2007

    Biomet RINGLOC + Instrumentation Impactor Plate, Size 22; REF/Part#: 31-400622, Biomet Orthopedics, Inc., Warsaw, IN.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·October 18, 2007

    Biomet RINGLOC + Instrumentation Impactor Plate, Size 23; REF/Part#: 31-400623, Biomet Orthopedics, Inc., Warsaw, IN.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LXH·October 18, 2007

    Vanguard PS Open Box Femoral 70 MM Left Interlock, " FOR CEMENTED USE ONLY" CO-CR-MO ALLOY. Biomet, Inc. A knee joint replacement prosthesis non-coated femoral indicated for cemented application only.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·July 6, 2011

    Biomet Vanguard DCM CR Tibial Bearing, 18MM x 71/75MM, CR STD bearing, sterile, Biomet Orthopedics, Inc., Warsaw, IN; Part 183448.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·February 12, 2008

    Biomet Vanguard DCM CR Tibial Bearing, 14MM x 79/83MM, CR STD bearing, sterile, Biomet Orthopedics, Inc., Warsaw, IN; Part 183464.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·February 12, 2008

    Biomet Orthopedics Apical Hole Plug, 3/8 - 24 threaded, TI-6AL-4V alloy, sterile; REF 123741, Biomet Orthopedics, Inc., Warsaw, IN 46581

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LPH·August 9, 2007

    Biomet --DCM AGC Molded Tibial Implant (12 mm x 80 mm)--Biomet Orthopedics , Interlok finish/posterior stabilized, 12 mm thick x 80 mm wide, UHMWPE/CO-CR-MO alloy, sterile; REF 155364, Biomet Orthopedic, Inc.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·July 24, 2007

    Biomet Vanguard Width Checker, Part Number: 32-487062, 67.5/75 Sizing Wing, Biomet Orthopedics, Inc., Warsaw, IN; The device is a preparatory instrument used for femoral knee insertion.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code HWT·February 12, 2008

    Biomet Interlok 67 mm Fixed Cruciate Tibial Plate with Locking Bar; CO-CR-MO/TI 6AL 4V Alloy; Product Number/REF 141232, Biomet Orthopedics, Inc., Warsaw, IN 46582

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·September 18, 2007

    BIOMET MICROFIXATION Trauma One SYSTEM 1.8X115 MM STOP DRILL, 1.8X115 MM WITH 26 MM STOP STAINLESS STEEL, NON-STERILE, BIOMET MICROFIXATION, INC. 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA.

    FDA Recall
    Terminated ·Biomet Microfixation, Inc.·Product code EJL·February 16, 2009

    Biomet Orthopedics, Vanguard PS Open Box Femoral, 67.5 mm Left-Interlok, For Cemented Use Only, CO-CR-MO Alloy, REF 183130, Knee Prosthesis Component, Biomet Orthopedics, Inc., Warsaw, IN 46581

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·August 31, 2007

    Biomet 5.5 mm peek Allthread PEEK Knotless Anchor, knotless, sterile, Biomet sports Medicine, Inc., Ontario, CA; REF 904842P. Intended to be implanted for fixation of bone fractures and for bone reconstructions.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code HWC·September 9, 2009