Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Select CAP Arterial Cannula Carmeda coated - Class 2 Recall
Medtronic Select CAP Arterial Cannulae. Non-Vented, Carmeda Coated, model CB78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Select 3D Arterial Cannulae has clear flexible, thin wall wire-wound PVC bodies with angled, beveled tips. The proximal end of the cannula includes a 3/8" (0.95 cm) vented or non-vented connector with a peel cap. The vented connector allows air to be vented from the cannula before connection to the perfusion line. The Select 3D Arterial Cannula tip has three integrated flutes which help diffuse and disperse blood flow. The cannula body features a tip orientation ...
Source: Medical Device Recalls - February 21, 2014 Category: Medical Equipment Source Type: alerts

Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Select CAP Arterial Cannula - Class 2 Recall
Medtronic Select CAP Arterial Cannulae. Vented, models 78818 (18 Fr.), 78820 (20 Fr.), 78822 (22 Fr.). Non-Vented Cannulae, model 78920 (20 Fr.), 78922 (22 Fr.), 78924 (24 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Cannula consists of a curved, angled or beveled tip with or without flange that is permanently attached to a molded, clear, flexible PVC tapered body or wirebound PVC body. The cannula body features a tip orientation line to indicate direction of the cannula tip during cannulation. The proximal end of the cannula includes a connection site or a molded 0.95 cm (3/8 in) barbed connector ...
Source: Medical Device Recalls - February 21, 2014 Category: Medical Equipment Source Type: alerts

Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Select 3D Arterial Cannula - Class 2 Recall
Medtronic Select 3D Arterial Cannulae. Vented, model 78624 (24 Fr.). Non-Vented Cannulae, model 78724 (24 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Cannula consists of a curved, angled or beveled tip with or without flange that is permanently attached to a molded, clear, flexible PVC tapered body or wirebound PVC body. The cannula body features a tip orientation line to indicate direction of the cannula tip during cannulation. The proximal end of the cannula includes a connection site or a molded 0.95 cm (3/8 in) barbed connector with or without a molded plastic vent plug or peel cap. The vent ...
Source: Medical Device Recalls - February 21, 2014 Category: Medical Equipment Source Type: alerts

Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Select 3D Arterial Cannula - Class 2 Recall
Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models 78718 (18 Fr.) and 78720 (20 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Select 3D Arterial Cannulae both have clear flexible, thin wall wire-wound PVC bodies with angled, beveled tips. The proximal end of the cannula includes a 3/8" (0.95 cm) vented or non-vented connector with a peel cap. The vented connector allows air to be vented from the cannula before connection to the perfusion line. The Select 3D Arterial Cannula tip has three integrated flutes which help diffuse an...
Source: Medical Device Recalls - February 21, 2014 Category: Medical Equipment Source Type: alerts

Integra LifeSciences Corp. - Class 2 Recall
Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra Neurosciences, 311 Enterprise Dr Plainsboro, NJ 08536 USA The Camino Advanced Monitor is a compact, portable device for use with Camino 110-4 series of Pressure / Temperature and Pressure Transducer-Tipped Catheters. Pressure and/or Temperature are measured at the Catheter tip, eliminating the need for external transducers, fluid, pressure tubing, and flush devices. The Camino displays intracranial pressure (ICP), intracranial temperature (ICT), and calculates cerebral perfusion pressure (CPP) (CPP = mean arterial pressure - mean intracranial pres...
Source: Medical Device Recalls - December 28, 2013 Category: Medical Equipment Source Type: alerts

GE Healthcare, LLC - HGE Healthcare Patient Monitor B30, Procare Monitor B20, Procare Monitor B40, and Monitor B40 - Class 2 Recall
HGE Healthcare Patient Monitor B30, Procare Monitor B20, Procare Monitor B40, and Monitor B40 K122253 (Procare Monitor B20): The PROCARE Monitor B20 is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and during intra-hospital transport. The PROCARE Monitor B20 is intended for use under the direct supervision of a licensed health care practitioner. The PROCARE Monitor B20 is not intended for use during MRI. The PROCARE Monitor B20 monitors and displays oscillometric n...
Source: Medical Device Recalls - December 13, 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

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, 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

Edwards Lifesciences, LLC - Edwards Duraflo coated Dispersion Tip Arterial Cannulae - Class 2 Recall
Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo Coating, Sterile, RX only For Single Use Only, Product Usage: Aortic perfusion cannulae are intended for perfusion of the ascending aorta during short-term (< 6 hours) cardiopulmonary bypass procedures. Aortic cannulae in sizes 6Fr to 18Fr can be used in pediatric patient populations. Extracorporeal circuit components with a Duraflo coating are intended for use in cardiopulmonary surgery when a heparin coated blood path is desired. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 2, 2013 Category: Medical Equipment Source Type: alerts

Edwards Lifesciences, LLC - Edwards Lifesciences EMBOLX Glide Protection System - Class 1 Recall
Edwards Lifesciences EMBOL-X Glide Protection System; Model Numbers: EXGF24D, EXGF24LLD, EXGF24MMD, EXGF24SSD, EXGF24XLD, EXGF24XSD, EXGFXS2D, EXGF24SS2D, EXGF24MM2D, EXGF24LL2D and EXGF24XL2D. The EMBOL-X access device is indicated for the perfusion of the ascending aorta during short-term (less than or equal to0¿ 6 hours) cardiopulmonary bypass (CPB) surgery where procedures may require the hemostatic introduction and removal of compatible intravascular devices into the vascular system. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 1, 2013 Category: Medical Equipment Source Type: alerts

Philips Medical Systems (Cleveland) Inc - Ingenuity TF PET/CT - Class 2 Recall
Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile installations that combines Positron Emission Tomography (PET) and X-Ray Computed Tomography (CT) systems. The CT subsystem produces cross sectional images of the body by computer reconstruction of x-ray transmission data. The PET subsystem produces images of the distribution of PET radiopharmaceuticals in the patient body (specific radiopharmaceuticals are used for whole body, brain, heart and other Oran imaging). Attenuation correction is accomplished by CTAC. The device also provides for list mode, dynamic, and gated acquisitions. Image processing and ...
Source: Medical Device Recalls - October 26, 2013 Category: Medical Equipment Source Type: alerts

Boston Scientific Corporation - Boston Scientific, FlextomeTM Cutting BalloonTM - Class 2 Recall
Boston Scientific, FlextomeTM Cutting BalloonTM, Sterilized using irradiation: 1) 4.00mm x 15mm FlextomeTM Cutting BalloonTM MonorailTM Microsurgical Dilatation Device, UPN #H749CBM3400150 Catalogue # CBM340015 & UPN# H749RB4400150 Catalogue # RB440015 2) 4.00mm x 15mm FlextomeTM Cutting BalloonTM Over-the-Wire Microsurgical Dilatation Device, UPN # H749CBO3400150, Catalogue # CBO340015 The Flextome Cutting Balloon Device is indicated for dilatation of stenoses in coronary arteries for the purpose of improving myocardial perfusion in those circumstances where a high pressure balloon resistant lesion is enco...
Source: Medical Device Recalls - September 4, 2013 Category: Medical Equipment Source Type: alerts

Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Custom Perfusion System with Trillium BioSurface - Class 2 Recall
Medtronic Custom Perfusion System with Trillium BioSurface (a polymer containing non-leaching heparin). Model Numbers: TL4X17R8, TL5D01R, TL5D02R, TL5D02R3, TL5D02R5, and TL6A65R7. 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

Medtronic Inc. Cardiac Rhythm Disease Management - Medtronic Custom Perfusion System - Class 2 Recall
Medtronic Custom Perfusion System. Model Numbers: 1D80R8, 1E34R1, 1F75R1, 1G49R2, 1G75R1, 1P07R8, 1P91R4, 5B15R11, and 5P51R9. Sterilized by Ethylene Oxide, Do no Reuse. Product 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