BEUDAMED
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    SINGLE USE ELECTROSURGICAL KNIFE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·June 6, 2022

    SINGLE USE ELECTROSURGICAL KNIFE KD-650

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·June 6, 2022

    EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 6, 2022

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 1, 2025

    EVIS LUCERA ELITE COLONOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDF·May 1, 2023

    EVIS LUSERA COLONOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDF·May 1, 2023

    GE Nuclear Medicine 600/800 series systems, specifically: a) 850, b) 850 / Dismount, c) 850 3/8 inch NM Gantry, d) 860 / Dismount, e) 860 3/8 inch NM Gantry, f) 860 5/8 inch NM Gantry, g) 860 BJ, h) NM 830 3/8 inch BJ, i) NM/CT 850 3/8 inch BJ, j) NM/CT 850 3/8 inch ROW, k) NM/CT 850 3/8 inch ROW_, l) NM/CT 850 CT 850 3/8 inch, m) NM/CT 850 ES 3/8 inch, n) NM/CT 850 ES 3/8 inch ROW, o) NM/CT 860 3/8 inch, p) NM/CT 860 3/8 inch BJ, q) NM/CT 860 3/8 inch ROW, r) NM/CT 860 ADVANCE, s) NM/CT 860 advance 3/8 inch NM Gantry, t) NM/CT 860 BEYOND, u) NM/CT 860 beyond 3/8 inch NM Gantry, v) NM/CT 860 China for China, w) NM/CT 860 CT 860 3/8 inch, x) NM/CT 860 ES 3/8 inch, y) NM/CT 860 ES 3/8 inch ROW, z) NM/CT 850 3/8 inch, aa) NM/CT 850 ES 3/8 inch ROW, bb) NM/CT 860 3/8 inch CH, cc) XELERIS 4 DR WORKSTATION; Emission Computed Tomography System

    FDA Recall
    Open, Classified ·GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING 4, Hayozma St Tirat Carmel Israel·Product code KPS·December 19, 2022

    CONTIGEN® BARD® COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code LNM·October 14, 2016

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·November 11, 2016

    CONTIGEN® BARD® COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code LNM·October 4, 2016

    CONTIGEN BARD® COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code LNM·August 11, 2015

    SOLESTA

    FDA Adverse Event
    Injury ·SALIX PHARMACEUTICALS, INC·Product code LNM·September 25, 2015

    CONTIGEN® BARD® COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code LNM·August 19, 2015

    CONTIGEN BARD COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code LNM·August 25, 2015

    DEFLUX INJECTABLE GEL

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·February 22, 2012

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LNM·January 30, 2012

    CONTIGEN BARD COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code LNM·March 21, 2012

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Injury ·BIOFORM MEDICAL, INC.·Product code LNM·February 18, 2009

    TEGRESS URETHRAL IMPLANT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code LNM·May 21, 2014

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·April 7, 2014