321 results
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39ms
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Sources: EU EUDAMED, US FDA
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Centros(TM) 15F x 24cm Chronic Hemodialysis Curved Catheter Set (With Cuff 19cm From Tip), Catalog No./REF 10303101. Sterile. Manufactured for AngioDynamics, Inc. MANUFACTURED IN USA. ANGIODYNAMICS, INC. Queensbury, NY USA 12804.
FDA Recall
Terminated
·Angiodynamics, Inc.·Product code MSD·July 7, 2008
Centros(TM) 15F x 28cm Chronic Hemodialysis Curved Catheter Set (With Cuff 23cm From Tip), Catalog No./REF 10303102. Sterile. Manufactured for AngioDynamics, Inc. MANUFACTURED IN USA. ANGIODYNAMICS, INC. Queensbury, NY USA 12804.
FDA Recall
Terminated
·Angiodynamics, Inc.·Product code MSD·July 7, 2008
Centros(TM) 15F x 32cm Chronic Hemodialysis Curved Catheter Set (With Cuff 27cm From Tip), Catalog No./REF 10303103. Sterile. Manufactured for AngioDynamics, Inc. MANUFACTURED IN USA. ANGIODYNAMICS, INC. Queensbury, NY USA 12804.
FDA Recall
Terminated
·Angiodynamics, Inc.·Product code MSD·July 7, 2008
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept guidewire: .035 in. --- Catalog No. [REF]: 10734201. Packaged in boxes of 5 catheters each, with manufacturer listed as AngioDynamics, Inc., Queensbury, NY USA. Intended use: angiographic diagnosis.
FDA Recall
Terminated
·Angiodynamics Worldwide Headquarters·Product code DQO·June 15, 2012
LifePort, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816.
FDA Recall
Terminated
·Angiodynamics, INC·Product code FRN·September 27, 2010
Habib, 4x Kit, Bipolar Resection Device RITA (Radiofrequency Ablation Devices). AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816. Intended to be used to assist in coagulation of tissue during intraoperative surgical procedures.
FDA Recall
Terminated
·Angiodynamics, INC·Product code GEI·August 30, 2010
Habib, 4x Kit, Bipolar Resection Device RITA (Radiofrequency Ablation Devices). AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816. Intended to be used to assist in coagulation of tissue during intraoperative surgical procedures.
FDA Recall
Terminated
·Angiodynamics, INC·Product code GEI·August 30, 2010
Vortex TR, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816
FDA Recall
Terminated
·Angiodynamics, INC·Product code FRN·September 27, 2010
Vortex LP, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816
FDA Recall
Terminated
·Angiodynamics, INC·Product code FRN·September 27, 2010
Triumph-1, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816.
FDA Recall
Terminated
·Angiodynamics, INC·Product code FRN·September 27, 2010
RITA StarBurst (2-3cm Diameter/25cm Length), Electro-surgical Device, Manufactured by: RITA Medical Systems, Inc., One Horizon Way, Manchester, GA 31816
FDA Recall
Terminated
·Rita Medical Systems, Inc.·Product code GEI·April 3, 2007
RITA Starburst MRI SemiFlex (3-5 cm Diameter/25cm Length), Electro-surgical Device, Manufactured by: RITA Medical Systems, Inc., One Horizon Way, Manchester, GA 31816
FDA Recall
Terminated
·Rita Medical Systems, Inc.·Product code GEI·April 3, 2007
RITA Starburst XL (3-5 cm Diameter/25cm Length), Electro-surgical Device, Manufactured by: RITA Medical Systems, Inc., One Horizon Way, Manchester, GA 31816
FDA Recall
Terminated
·Rita Medical Systems, Inc.·Product code GEI·April 3, 2007
SmartPort CT Port Access System, Catalog number CT80STPD, AngioDynamics Incorporated The SmartPort CT Port Access System is indicated for any patient requiring repeated access of the vascular system or other selected body site, for delivery of medications, nutritional supplementation, fluids, blood products, and sampling of blood.
FDA Recall
Terminated
·Angiodynamics, INC·Product code LJT·July 16, 2009
Vortex VX Port, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816
FDA Recall
Terminated
·Angiodynamics, INC·Product code FRN·September 27, 2010
Vortex MP Port Single Titanium Port with Attached (5Fr) Silicone Catheter, AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816 Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling.
FDA Recall
Terminated
·Angiodynamics, INC·Product code LJT·August 30, 2010
ANGIODYNAMICS BENEPHIT(TM) XT Infusion System, 35 cm, Targeted Renal Therapy Infusion system, Model/REF Number 70035, STERILE, EO, Intended for Single Use Only. AngioDynamics, Incorporated 603 Queensbury, NY 12804.
FDA Recall
Terminated
·Angiodynamics, Inc.·Product code KRA·April 30, 2010
Vortex MP Port Single Titanium Port with Attachable (5Fr) Silicone Catheter, AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816 Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling.
FDA Recall
Terminated
·Angiodynamics, INC·Product code LJT·August 30, 2010
ANGIODYNAMICS Angiographic Catheter, Soft-Vu Cobra (2) BRAIDED, 5 F x 90 cm x .035 in., Catalog No./REF 10709105, STERILE, MANUFACTURED IN USA, AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804 Angiographic catheter
FDA Recall
Terminated
·Angiodynamics Worldwide Headquarters·Product code DQO·June 7, 2011
AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit, Sterile, Catalog Number: 06597005, 2) AngioDynamics 5F Standard Micro-Introducer Kit, Sterile, Catalog number: 06597012; 3) AngioDynamics 4F Standard Micro-Introducer Kit, Sterile, Catalog Number: 06597013; 4) AngioDynamics 5F Standard Micro- Introducer Kit, Sterile, Catalog Number: 06597018; and 5) AngioDynamics 4F Standard Micro-Introducer Kit, Sterile, Catalog Number: 06597019. Product kits are individually wrapped in plastic, 10 units included per box. Product Usage: This device is intended to be used to measure the refractive power and the radius of corneal curvature of the human eye.
FDA Recall
Terminated
·Angiodynamics, Inc.·Product code DQR·April 30, 2013