BEUDAMED
    39 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall ×

    Hemashield Gold Woven and Knitted Double Vascular Grafts.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code MAL·May 24, 2010

    Hemashield Platinum Woven Double Velour TAAA Vascular Grafts.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code MAL·May 24, 2010

    Hemashield Gold Woven Double Velour Vascular Branch Graft

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DSY·May 24, 2010

    Hemashield Double Velour Cardiovascular Fabrics.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DXZ·May 24, 2010

    Hemashield Finesse Ultra-thin Knitted Cardiovascular Patch.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DSZ·May 24, 2010

    Hemashield Platinum Woven and Knitted Double Velour Vascular Grafts.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code MAL·May 24, 2010

    Heartstring II Proximal Seal / VASOVIEW 6 Endoscopic Vessel Harvesting System, Model Number: VH-2000, Product is manufactured and distributed by Maquet Corporation San Jose, CA

    FDA Recall
    Terminated ·CTS, Inc. dba Guidant Cardiac Surgery·Product code GCJ·February 5, 2009

    VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code GEI·September 20, 2024

    Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code GEI·September 19, 2023

    Heartstring III Proximal Seal System. Intravascular anastomosis occluder.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DXC·August 15, 2025

    Heartstring III Proximal Seal System, 4.3 MM. Intravascular anastomosis occluder.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DXC·August 15, 2025

    Heartstring III Proximal Seal System, 3.8 MM. Intravascular anastomosis occluder.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DXC·August 15, 2025

    Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DWS·February 9, 2022

    Maquet HEARTSTRING Aortic Cutter 4.3 mm, AC-3043, Lot numbers 9081071 and 9082071, Manufactured by Maquet Cardiovascular, Wayne, New Jersey. Intended for use by cardiac surgeons during CABG procedures to create an opening in the wall of a vessel.

    FDA Recall
    Terminated ·Maquet Cardiovascular·Product code FZT·June 4, 2010

    EXXCEL Soft Standard Wall EPTFE Vascular Graft; D:8 mm; L: 50 cm straight. Sterile Intended use: The Standard Wall EXXCEL and EXXCEL Soft ePTFE Vascular Grafts are designed to repair or replace peripheral arteries and to provide vascular access. Wall Soft ePTFE Vascular Grafts are designed to repair or replace peripheral arteries.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DSY·March 26, 2010

    Maquet Heartstring II Proximal Seal System (HS-1045) manufactured by Maquet Cardiovascular, Wayne, NJ Intended use: medical device for use by cardiac surgeons during CABG procedures to maintain hemostasis and to facilitate the completion of a proximal anastomosis without application of an aortic clamp.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DXC·May 5, 2010

    EXXCEL Soft Thin Wall EPTFE Vascular Graft; D:8 mm; L: 50 cm straight. Sterile Intended use: The Standard Wall EXXCEL and EXXCEL Soft ePTFE Vascular Grafts are designed to repair or replace peripheral arteries and to provide vascular access. Wall Soft ePTFE Vascular Grafts are designed to repair or replace peripheral arteries.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DSY·March 26, 2010

    VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System; Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally invasive surgery allowing access for vessel harvesting and are primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code GEI·December 17, 2009

    VASOVIEW 7xB Endoscopic Vessel Harvesting System; Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally invasive surgery allowing access for vessel harvesting and are primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code GEI·December 17, 2009

    VASOVIEW 6 Endoscopic Vessel Harvesting System Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally invasive surgery allowing access for vessel harvesting and are primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code GEI·December 17, 2009