116 results · 18ms · Sources: EU EUDAMED, US FDA

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ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 120mm x 135cm, REF: AB35W06120135. and ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 40mm x, 80cm REF: AB35W06040080. Peripheral Dilatation Catheter

FDA Recall
Terminated ·Product code DQY·April 9, 2014

Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature.

FDA Recall
Terminated ·Abbott Vascular·Product code LIT·August 20, 2012

Pacific Xtreme (PTCA Balloon Dilation Catheter)

FDA Recall
Terminated ·Product code LIT·August 26, 2020

Boston Scientific, 2.5mm Coyote" OVER-THE-WIRE PTA Balloon Dilation Catheter, UPN# H74939186251210, Catalog # 39186-25121.

FDA Recall
Terminated ·Boston Scientific Corporation·Product code LIT·February 4, 2014

Boston Scientific, Coyote" MONORAIL" PTA Balloon Dilatation Catheter, UPN # H74939185201510, Catalogue # 39185-20151.

FDA Recall
Terminated ·Boston Scientific Corporation·Product code LIT·February 4, 2014

Hermes NC PTA Balloon Dilatation Catheter The balloon dilatation catheter is intended to dilate stenoses in the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for stent dilatation post-deployment in the peripheral vasculature.

FDA Recall
Terminated ·BrosMed Medical Co., Ltd. Bubugaogaofu Lou Lou 15th Songshan Lake Hi Dongguan China·Product code LIT·December 14, 2018

ANGIODYNAMICS PROFILER BALLOON DILATATION CATHETER, Catalog No./REF 16801101, BALLOON DIAMETER 4MM, BALLOON LENGTH 2 CM, CATHETER LENGTH 40 CM, STERILE, MANUFACTURED IN USA AngioDynamics 603 Queensbury Avenue, Queensbury, NY 12804 Cardiovascular catheterization

FDA Recall
Terminated ·Angiodynamics Worldwide Headquarters·Product code DQY·February 25, 2011

ANGIODYNAMICS PROFILER BALLOON DILATATION CATHETER, Catalog No./REF 16801105, BALLOON DIAMETER 5MM, BALLOON LENGTH 4 CM, CATHETER LENGTH 40 CM, STERILE, MANUFACTURED IN USA AngioDynamics 603 Queensbury Avenue, Queensbury, NY 12804 Cardiovascular catheterization

FDA Recall
Terminated ·Angiodynamics Worldwide Headquarters·Product code DQY·February 25, 2011

USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.

FDA Recall
Terminated ·Us Endovascular·Product code LIT·February 11, 2016

ev3, PowerCross" 0.018" OTW PTA Dilatation Catheter, model: AB18W030200150, Sterile EO, Rx Only.

FDA Recall
Terminated ·ev3, Inc.·Product code LIT·March 29, 2016

BARD PERIPHERAL VASCULAR VACCESS PTA Balloon Dilatation Catheters, 8mm x 4cm x 80cm. Product Usage: Vaccess PTA Balloon Dilatation Catheters are recommended for use in Percutaneous Transluminal Angioplasty of the femoral, iliac and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also recommended for post-dilatation of balloon expandable stents, self-expanding stents and stent grafts in the peripheral vasculature. This catheter is not for use in coronary arteries. Vaccess PTA Balloon Dilatation Catheters are supplied sterile and intended for single use.

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 28, 2013

Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S

FDA Recall
Terminated ·Cordis Corporation·Product code LIT·January 8, 2020

Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152 AMP020150152 AMP025120152 AMP030080152 AMP040040152 AMP225210152 AMP020040152 AMP025040152 AMP025150152 AMP030120152 AMP040080152 AMP253210152 AMP020080152 AMP025080002 AMP030040002 AMP030150152 AMP040120152 AMP335210152 AMP020120152 AMP025080152 AMP030040152 AMP035120152 AMP040150152 AMP354210152; OUS: AMD025150152 AMD030150152 AMD040120002 AMD335210002 AMD030040002 AMD035040152 AMD040120152 AMD335210152 AMD030040152 AMD035120002 AMD040150002 AMD354210002 AMD030080002 AMD035150002 AMD040150152 AMD354210152 AMD030080152 AMD035150152 AMD225210002 AMD030120002 AMD040040152 AMD225210152 AMD030120152 AMD040080002 AMD253210002 AMD030150002 AMD040080152 AMD253210152 Cardiovascular: Intended for use in Angioplasty

FDA Recall
Terminated ·Medtronic Vascular, Inc.·Product code DQY·October 23, 2015

ev3, PowerCross .018 OTW PTA Dilatation Catheter, Sterile EO. The PowerCross .018 OTW PTA Dilatation Catheter is intended to dilate stenoses in the iliac, femoral, ilio-femoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for stent post-dilatation in the peripheral vasculature.

FDA Recall
Terminated ·Medtronic Inc·Product code LIT·November 10, 2016

Advance 35LP Low-Profile PTA Balloon Dilatation Catheter; Catalog numbers: PTA5-35-135-6-2 .0 and PTA5-35-135-4-4 .0; UDI: 10827002522647 and 10827002522524 Product Usage: The Advance 35LP Low Profile PTA Balloon Dilation Catheter is indicated for percutaneous transluminal angioplasty (PTA) of lesions in peripheral arteries including iliac, renal, popliteal, infrapopliteal, femoral and iliofemoral as well as obstructive lesions of native or synthetic arteriovenous dialysis fistulae.

FDA Recall
Terminated ·Cook Inc.·Product code DQY·April 16, 2018

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135417

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135615

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135715

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135512

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135612

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010