BEUDAMED
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    JDL Sensitive

    FDA UDI
    Surgyco LLC·10850074089022·JDL Sensitive Nitrile Examination Gloves Medium

    JDL Sensitive

    FDA UDI
    Surgyco LLC·10850074089015·JDL Sensitive Nitrile Examination Gloves Small

    JDL Sensitive

    FDA UDI
    Surgyco LLC·10850074089039·JDL Sensitive Nitrile Examination Gloves Large

    JDL Sensitive

    FDA UDI
    Surgyco LLC·10850074089046·JDL Sensitive Nitrile Examination Gloves X-large

    SNAP-RING FOR 52MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 4, 2007

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT

    FDA Adverse Event
    Death ·BOSTON SCIENTTIFIC·Product code NIQ·June 8, 2006

    Crossfire Acetabular II Insert. Catalog No: 2041C-2642.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics·Product code JDL·January 9, 2004

    CONSERVE, TOTAL A-CLASS HEAD W/BFH TECH., REF 38AM-3635, O.D. Size: 36mm, Neck Length: +3.5mm, Taper: SLT, Sterile R, 1 each, Rx only, Wright Medical Technology, Inc., 5677 Airline, Road, Arlington, TN 38002. The CONSERVE Total Femoral Head is indicated for use in total hip arthroplasty for reduction of relief of pain and/or improved hip function in skeletally mature patients.

    FDA Recall
    Terminated ·Wright Medical Technology Inc·Product code JDL·May 14, 2009

    DYNASTY A-CLASS POLY LINER, REF DLXP-LD36, 1 EACH, Rx ONLY, STERILE EO, GROUP D, I.D. 36 mm, LIP 15o, LINER STD, Wright Medical Technology, 4677 Airline Road, Arlington, TN 38002. Product is used in total hip arthroplasty.

    FDA Recall
    Terminated ·Wright Medical Technology Inc·Product code JDL·June 7, 2010

    CONSERVE, TOTAL A-CLASS HEAD W/BFH TECH., REF 38AM-3604, O.D. Size: 36mm, Neck Length: -3.5mm, Taper: SLT, Sterile R, 1 each, Rx only, Wright Medical Technology, Inc., 5677 Airline, Road, Arlington, TN 38002. The CONSERVE Total Femoral Head is indicated for use in total hip arthroplasty for reduction of relief of pain and/or improved hip function in skeletally mature patients.

    FDA Recall
    Terminated ·Wright Medical Technology Inc·Product code JDL·May 14, 2009

    C2A / M2A SYSTEM W/PLUG 52MM O.D. SHELL SIZE 41MM I.D. TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDL·October 19, 2016

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·October 20, 2016

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·November 3, 2016

    LINEAGE(R) TRANSCEND(R) SUPERFINISHED FEMORAL HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·October 5, 2016

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·December 30, 2016

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 10, 2015

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 21, 2015

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·August 24, 2015

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 23, 2015

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 8, 2015