Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Custom Perfusion System - Class 2 Recall
Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model Numbers: CB1D82R12 and CB5N73R7. Sterilized by Ethylene Oxide, Do no Reuse. Product Usage: Usage: This product is indicated for use in the extracorporeal circuit during cardiopulmonary surgery. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 28, 2013 Category: Medical Equipment Source Type: alerts

Sorin Group USA, Inc. - Edwards Lifesciences Suction Wand Model S099B - Class 2 Recall
Edwards Lifesciences Suction Wand Model S099B, packaged in Sorin Group Heart/Lung Perfusion Packs. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 21, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Terumo Advanced PErfusion System 1 - Class 2 Recall
100/120V AC, Advanced Perfusion System 1 Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the operation of Sarns TM or similar equipment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 16, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo¿ Advanced Perfusion System 1: 100/120V AC, Advanced Perfusion System 1 The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the operation of Sarns " or similar equipment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 15, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo¿ Advanced Perfusion System 1: 220/240V AC, Advanced Perfusion System 1 The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the operation of Sarns " or similar equipment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 15, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo¿ Advanced Perfusion System 1 (APS1, System 1) Description: 220/240V AC Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the operation of Sarns TM or similar equipment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 15, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo¿ Advanced Perfusion System 1 (APS1, System 1) 100/120V AC Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the operation of Sarns TM or similar equipment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 15, 2013 Category: Medical Equipment Source Type: alerts

Vital Images, Inc. - Vitrea - Class 2 Recall
Vitrea¿ CT Brain Perfusion made available in various configurations under the names Vitrea, Vitrea fX, VitreaAdvanced and Vitrea Enterprise Suite. Noninvasive post-processing application designed to evaluate areas of brain perfusion. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 27, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns highflow aortic arch cannula - Class 2 Recall
Sarns high-flow aortic arch cannula, 6.5 mm (20 Fr) OD with 3/8in connector, 11in (28 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns flexible arterial cannula - Class 2 Recall
Sarns flexible arterial cannula, 6.7 mm (20Fr) OD with 3/8 in. connector, suture ring, 9.5 in (24 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns highflow aortic arch cannula - Class 2 Recall
Sarns high-flow aortic arch cannula, 5.2 mm (16 Fr) OD with 3/8in connector, 7.5in (19 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns flexible arterial cannula - Class 2 Recall
Sarns flexible arterial cannula, 8.0 mm (24 Fr) with 3/8in connector, suture ring, 9.5in (24 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns highflow aortic arch cannula - Class 2 Recall
Sarns high-flow aortic arch cannula, 6.5 mm (20 Fr) OD with 3/8in connector, 11in (28 cm) long, with X coating surface The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2013 Category: Medical Equipment Source Type: alerts

Terumo Cardiovascular Systems Corporation - Sarns flexible arterial cannula - Class 2 Recall
Sarns flexible arterial cannula, 7.3 mm (22 Fr) OD with 3/8in connector, suture ring, 9.5in (24 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2013 Category: Medical Equipment Source Type: alerts