BEUDAMED
    56 results · 14ms · Sources: EU EUDAMED, US FDA

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    BNX Fine Need Aspiration System (22GA); Material/Part#: DSN-22-01

    FDA Recall
    Terminated ·Medtronic·Product code FCG·February 8, 2017

    BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01

    FDA Recall
    Terminated ·Medtronic·Product code FCG·February 8, 2017

    (1) JOBST Compri2, REF 76271-01, containing 2 components, one plastic-wrapped padding and one plastic-wrapped compression bandage with compression of approximately 40 mmHg packaged into a pouch and then both components are packaged into a folding box. Shipping case contains 10 folding boxes. (2) JOBST Compri2 lite, REF 76271-02, containing 2 components, one plastic-wrapped padding (as is contained in REF 76271-01) and one plastic wrapped compression bandage with a compression of approximately 20-30mmHg packaged into a pouch and then both components are packaged into a folding box. Shipping case contains 10 folding boxes.

    FDA Recall
    Terminated ·BSN Medical Inc·Product code FQM·February 1, 2022

    3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3, 1590S-1, 1590S-2, 1590B-118, 1590B-136

    FDA Recall
    Terminated ·3M Company Health Care Business 3m Center·Product code KGX·November 21, 2019

    VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of non-liquid interventional devices (such as stents/flow diverters) and infusion of diagnostic (such as contrast media) or therapeutic agents into the neuro, peripheral, and coronary vasculature. The catheter is inserted into the body through a small puncture made in the skin and into a blood vessel. The VIA 27 Microcatheter is contraindicated for use with liquid embolic materials, such as n-butyl 2-cyanoacrylate or ethylene vinyl alcohol & DMSO (dimethyl sulfoxide).

    FDA Recall
    Terminated ·Sequent Medical Inc·Product code KRA·September 23, 2016

    Unicel DxC 600i System and Unicel Dxl 600 Access Immunoassay System

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code CFR·April 3, 2008

    Access and Access 2 Immunoassay System

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code CGN·April 3, 2008

    UniCel Dxl 800 Access Immunoassay System and UniCel DxC 880i Synchron Access Clinical System

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code JJE·April 3, 2008

    SYNCHRON LXi 725 System

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code JGS·April 3, 2008

    Private Eyes, Diam 14.0 BC 8.6, Contents: one sterile daily wear soft contact lenses, 38% water, 62% polymacon, immersed in 0.9% buffered saline solution USP, Manufactured by Soft Lens Technology, Lot BB43 Expiration Date 08/06, Cosmetic Use Daily Wear ***Decorative Theatrical Contact Lenses, packed in vials labeled sterile. Types include: Zombie, Banshee, Green Leaf, Green Reptile, White Cat, Manson, Green Rave, Moon & Stars, Blackwolf, Fire, Black Out, Pink Rave, Spiral, Flower Power, Starfire, Yellow Cat Eye, Computer Chip, Target, Red Cat, Blue Rave, Smiley, White Snowflake and Red Vampire..

    FDA Recall
    Terminated ·The Contact Lens Store, Inc.·Product code LPL·June 7, 2004

    200996-Cable Assembly, Hybrid Extended Length, 200997 Cable Assembly, Hybrid, Guidance Module, 200998 Cable Assembly, Hybrid, UI Panel Subcomponents for the 203000 RIO STANDARD SYSTEM Manufactured by: MAKO Surgical, Corp. Fort Lauderdale, FL. All three cables are integral components and are not purchased separately. However, 200996-Cable Assembly is the only cable visible. This cable is labeled: 200996-REV-1, KSM 390634-1, SN 000001. 200997 and 200998 Cable Assembly are not visible . The Tactile Guidance System v2.0 is intended to assist the surgeon in providing software defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.

    FDA Recall
    Terminated ·Mako Surgical Corporation·Product code HAW·July 17, 2009

    Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562

    FDA Recall
    Terminated ·Galemed Corporation 87 Wu-Jia Li-Gong 2nd Road I-Lan Taiwan·Product code BZD·May 30, 2019

    Babi.Plus 12.5 cm H2O Pressure Relief Manifold with Gas Supply Tube and Oxygen Sensor Port, REF 2691, Rx Only, UDI: 04710810100802

    FDA Recall
    Terminated ·Galemed Corporation 87 Wu-Jia Li-Gong 2nd Road I-Lan Taiwan·Product code BZD·May 30, 2019

    Babi.Plus Bubble PAP Valve with 12.5 cm H2O Pressure Relief Manifold, REF 1002, Rx Only, UDI: 24710810093559

    FDA Recall
    Terminated ·Galemed Corporation 87 Wu-Jia Li-Gong 2nd Road I-Lan Taiwan·Product code BZD·May 30, 2019

    INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS

    FDA Recall
    Terminated ·Wright Medical Technology Inc·Product code HSN·November 4, 2021

    Talar Dome Total Ankle Prosthesis, Flat Cut, Size 3, Right, Product No. LJU813T

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code HSN·March 8, 2019

    Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code HSN·March 8, 2019

    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 1, Left, Part No. LJU211T

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code HSN·March 8, 2019

    Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Right, Product No. LJV180T

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code HSN·March 8, 2019

    Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code HSN·March 8, 2019