BEUDAMED
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    SURGITEK FOERSTER FACE LIFT BANDAGE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Helix

    FDA UDI
    Nuvasive, Inc.·00887517135551·Helix R Plate, 48mm 2-Level

    HEARTLINE COOLEY SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896007062·HEARTLINE COOLEY SCISSORS CURVED BLADE TUNGSTEN...

    ACUMED

    FDA UDI
    Acumed LLC·10806378040641·Small Plate Tack

    KETAC-CEM IN REF. TO K802048

    FDA 510(k)
    FDA Class 2 ·Dental

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197491365·Malleable Retractor Blade, with lip 38x168...

    CARTO EP NAVIGATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPECTRA VRMIII Q-SWITCHED ND: YAG LASER SYSTEM AND DYE HANDPIECES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MICROCLAVE® NEUTRAL CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·December 15, 2022

    3 LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·CENTURION 1-800-248-5068·Product code DYB·July 7, 2017

    STANDARD IM NAIL

    FDA Adverse Event
    Injury ·SIGN FRACTURE CARE INTERNATIONAL·Product code HSB·April 30, 2014

    GOBED+

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·October 8, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 31, 2007

    FEM. MODULAR HEAD - L Ø36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code LZO·February 6, 2019

    Material DT7890, PORT ACCESS TRAY, CENTURION HEALTHCARE PRODUCTS PORT ACCESS TRAY, REORDER DT7890, STERILE, TRI-STATE HOSPITAL SUPPLY Manufacturers of CENTURION Healthcare Products Howell, MI 48843 USA (800) 248-4058 www.tshsc.com FACILITATES PORT INSERTION

    FDA Recall
    Terminated ·Centurion Medical Products Corporation·Product code MCY·March 31, 2011

    AIA-360 Automated Immunoassay Analyzer, Product Code 019945

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code KHO·January 10, 2020

    ST AIA-PACK PROG III, Progesterone III Assay, Part Number: 025240

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code JLS·February 13, 2018

    ST AIA-PACK PROG II, Progesterone II Assay, Part Number: 025239

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code JLS·February 13, 2018

    ST-AIA PACK LH II; Part Number: 025296 Assay, Reproductive Hormone

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code CEP·March 5, 2018

    ST-AIA PACK PA; Part Number: 025263 Assay, Tumor Marker

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code LTJ·March 5, 2018