BEUDAMED
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    Filters FDA Recall × Status: Terminated × Clear all

    daVinci S Surgical system, patient side cart Auxiliary power board (APB) (printed circuit board assembly), endoscopic instrument control system.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 14, 2007

    Medtronic Performer CPB-Universal R2100375. Catologue Number R5100052. The Performer CPB System is an electromechanical extracorporeal support device used during cardiopulmonary bypass procedures. Manufactured by: RanD S.r.l 41036 Mendolla (MO) Italy. Distributed exclusively by Medtronic, Inc.

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DTQ·June 4, 2007

    Maquet Getinge-BEQ-TOP 30901 CUSTOM CPB PACK Material:701063071

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

    Maquet Getinge-BO-TOP 30901 CUSTOM CPB PACK Material: 701055372

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

    Maquet Getinge-BEQ-T 4906 PEDIARIC CPB PACK Material: 701056041

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

    BPB medica CEMIX, PRODUCT NUMBER KVTMIXN, Vertebroplasty-Kyphoplasty cement mixing system

    FDA Recall
    Terminated ·BIOPSYBELL S.R.L. Via Aldo Manuzio N. 24 Via A.Manuzio n.24 Mirandola Italy·Product code LOD·March 22, 2021

    BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT, 110 mm, 11 G, REF OBE1111

    FDA Recall
    Terminated ·BIOPSYBELL S.R.L. Via Aldo Manuzio N. 24 Via A.Manuzio n.24 Mirandola Italy·Product code KNW·March 22, 2021

    BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP, 187 mm, 10G, RES RESWTR1112C-US

    FDA Recall
    Terminated ·BIOPSYBELL S.R.L. Via Aldo Manuzio N. 24 Via A.Manuzio n.24 Mirandola Italy·Product code LOD·March 22, 2021

    Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB) surgical procedures.

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DWF·January 3, 2018

    COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002

    FDA Recall
    Terminated ·AtriCure, Inc.·Product code OCL·January 22, 2019

    COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S

    FDA Recall
    Terminated ·AtriCure, Inc.·Product code OCL·January 22, 2019

    COBRA FUSION 150 Ablation System (International Only), Catalog # (REF) 700-001MI

    FDA Recall
    Terminated ·AtriCure, Inc.·Product code OCL·January 22, 2019

    COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001

    FDA Recall
    Terminated ·AtriCure, Inc.·Product code OCL·January 22, 2019

    CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corporation·Product code DWF·May 9, 2012

    CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corporation·Product code DWF·May 9, 2012

    CPB Catheter Kit Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corporation·Product code DWF·May 23, 2014

    Proton therapy system -Proteus 235 aka Proteus Plus. A medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

    FDA Recall
    Terminated ·Product code LHN·April 10, 2017

    Heartport Direct Flow Arterial Cannula, product code DFK24. The device is sold separately and also in the following Kit Model Numbers: EDNN241, EDnn242, EDNN243, and EDNN244.

    FDA Recall
    Terminated ·Ethicon, Inc. US·Product code DWF·April 27, 2006

    Medtronic Venous Cannula with bent tip wire, for vascular cardiopulmonary bypass. Catalog Number: CB67532

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DWF·May 9, 2008

    Medtronic Affinity Pediatric arterial Filter, Arterial Line Filter for Cardiopulmonary Bypass. Catalog Number: CB4014

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DTM·May 9, 2008