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Terumo Cardiovascular Systems Corporation - Sarns Malleable Dualstage Venous Return Cannulae - Class 2 Recall
Sarns Malleable Dual-stage Venous Return Cannulae, 28/38 Fr with 1/2" connector, 14.5" (37 cm) long The Sarns Malleable Dual-stage Venous Return Catheters and Sarns Dual-stage Venous Return Cannula are indicated for single-tube venous drainage from the right atrium and vena cava during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 20, 2014 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns Dualstage Venous Return Cannulae - Class 2 Recall
Sarns Dual-stage Venous Return Cannulae, 34/46 Fr with 1/2" flare The Sarns Malleable Dual-stage Venous Return Catheters and Sarns Dual-stage Venous Return Cannula are indicated for single-tube venous drainage from the right atrium and vena cava during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 20, 2014 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns Malleable Dualstage Venous Return Cannulae - Class 2 Recall
Sarns Malleable Dual-stage Venous Return Cannulae, 34/46 Fr with 1/2" connector, 15" (38 cm) long, with X Coating The Sarns Malleable Dual-stage Venous Return Catheters and Sarns Dual-stage Venous Return Cannula are indicated for single-tube venous drainage from the right atrium and vena cava during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 20, 2014 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns Malleable Dualstage Venous Return Cannulae - Class 2 Recall
Sarns Malleable Dual-stage Venous Return Cannulae, 34/46 Fr with 1/2" connector, 15" (38 cm) long The Sarns Malleable Dual-stage Venous Return Catheters and Sarns Dual-stage Venous Return Cannula are indicated for single-tube venous drainage from the right atrium and vena cava during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 20, 2014 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Electrosurgical Cutting and Coagulation Device - Class 2 Recall
VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System, Part number: VSP550, Sterile***Rx Only*** Product Usage: The VirtuoSaph Plus Endoscopic Vessel Harvesting System is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2014 Category: Medical Equipment Source Type: alerts

Medtronic Cardiovascular Surgery-the Heart Valve Division - Model 7305 Mosaic Aortic Obturator - Class 2 Recall
Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 4, 2014 Category: Medical Equipment Source Type: alerts

Maquet Cardiovascular, LLC - Vasoview Hemopro Endoscopic Vessel Harvesting System - Class 2 Recall
Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour Pond Drive Wayne, NJ 07470 Indicated for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. It is indicated for cutting tissue and controlling bleeding through coagulation, and for patients requiring blunt dissection of tissue including dissection of blood vessels, dissection of blood vessels oft he extremities, dissection of ducts and other structures int he extraperitoneal or subcutaneous extremity and thoracic space. ...
Source: Medical Device Recalls - December 7, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns SoftFlow Aortic Cannula without Suture Flange - Class 2 Recall
Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange, straight tip, wire-reinforced with luer port, aortic cannula, 7.0 mm (21 Fr) OD with 3/8" connector, 14" (36 cm) long. Indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 9, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns Venous Return Cannulae - Class 2 Recall
Sarns" Venous Return Cannulae, 20 Fr with 1/4" flare, 14.5" (37 cm) long. Indicated for venous drainage during cardiopulmonary bypass surgery for dial cannulation of the superior and inferior vena cava. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 9, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns SoftFlow Aortic Cannula without Suture Flange - Class 2 Recall
Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange, angled tip, wire-reinforced with luer port, aortic cannula, 8.0 mm (24 Fr) OD with 3/8" connector, 14" (36 cm) long. Indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 9, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns SoftFlow Aortic Cannula without Suture Flange - Class 2 Recall
Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange, straight tip, wire-reinforced with luer port, aortic cannula, 8.0 mm (24 Fr) OD with 3/8" connector, 14" (36 cm) long. Indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 9, 2013 Category: Medical Equipment Source Type: alerts

Maquet Cardiovascular, LLC - ULTIMA OPCAB System - Class 2 Recall
Ultima OPCAB System, Sterile, Rx Only, Product Usage: Intended for use during performance of minimally invasive cardiac surgery through a sternotomy incision approach. The ULTIMA Access RailPlatform in combination with the Activator II Drive Mechanism is used to spread the sternum, providing access and direct visualization to the thoracic cavity. The AccessRail Platform also allows for the organization of pericardial sutures. The ULTIMA Stablizer isolates and provides local immobilization of the target vessel on the beating heart. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2013 Category: Medical Equipment Source Type: alerts

Maquet Cardiovascular Us Sales, Llc - QUADROX Oxygenator - Class 2 Recall
QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-iD Pediatric HMOD 30000. The QUADROX oxygenators are intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 21, 2013 Category: Medical Equipment Source Type: alerts

Covidien LP - Covidien Endo GIA - Class 2 Recall
Covidien Endo GIA AutoSuture Universal Loading Unit, 30mm-2.0mm Product Code: 030450 Applications in abdominal, gynecologic, pediatric anti thoracic surgery for resection, transection and creation of anastomosis. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 6, 2013 Category: Medical Equipment Source Type: alerts

Healthtronics, Inc. - HealthTronics Endocare 3.8mm RenalCryo Cryoprobe - Class 2 Recall
HealthTronics Endocare 3.8mm RenalCryo Cryoprobe, R3.8L, Endocare, Inc., a wholly owned subsidiary of HealthTronics, Inc., 9825 Spectrum Dr. Building 3, Austin, TX 78717 The Endocare CryoProbe is an accessory probe intended for use with the CryoCare Surgical System. The CryoCare Surgical System is intended for use in surgical procedures in the arrears of general surgery, dermatology, neurology, thoracic surgery, pulmonary surgery, (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 16, 2013 Category: Medical Equipment Source Type: alerts