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Richard H. El Paso, Texas
I am an 81 year old retired general surgeon and have COPD. I have had a transtracheal catheter... More
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Mummy to Alina Houchin, dob 19/12/2008, diagnosed with congenital diaphramatic hernia at... More
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balloon catheter Blogs and DiscussionsArticles

 
AngioSculpt "EX" PTCA Scoring Balloon Catheter by AngioScore, Inc.: Recall - Risk of Catheter Separation by FDA Scoring Balloon Catheter is used to dilate narrowed coronary arteries (stenosis), and to improve blood...: The AngioSculpt EX Percutaneous Transluminal Coronary Angioplasty (PTCA) catheters may become separated...
Arrow Intra-Aortic Balloon (IAB) Catheter Products: Class 1 Recall - Catheters Can Become Stuck in the Sheath by FDA Ultra 8 Intra-Aortic Balloon Catheters (IABS) 8 FR 30CC and 40CC Universal and Arrow Intra-Aortic Balloon (IAB) Catheter with a Fiber Optic Sensor and a Measurement System are recalled...
AngioScore Incorporated Announces Worldwide Voluntary Field Removal of the AngioSculpt® PTA Scoring Balloon Catheter, 0.018 by FDA , CA initiated a worldwide recall of the AngioSculpt® PTA Scoring Balloon Catheter, 0.018” OTW, balloon... catheters, or any AngioSculpt PTA catheter balloon sizes (in millimeters): 0.014” OTW, 2.0x10, 2.0x20...
AngioScore Inc., AngioSculpt Percutaneous Transluminal Angioplasty (PTA) Scoring Balloon Catheter OTW 0.018" Platform - Class I by FDA : 2076-4020, 2076-5020, 2076-6020, 2092-6020, 2105-6020. BACKGROUND: The AngioSculpt PTA Scoring Balloon Catheter OTW 0.018" Platform is used for dilatation of lesions in the iliac, femoral, ilia-femoral...
Cook Medical Announces FDA Clearance for Advance® 35LP PTA Balloon Dilatation Catheter - PVD by Medical Quack Patient ExpertHealth Maven from the U.S. Food and Drug Administration (FDA) to market its newest balloon dilatation catheter, the Advance... of low-profile PTA balloons, provides physicians with enhanced deliverability to the superficial femoral...
Class I Medical Device Recall: Arrow Ultra 8 Intra-Aortic Balloon Catheters (IABS) 8 FR 30CC and 40CC Universal and Arrow Intra- by FDA , 40cc Arrow Intra-Aortic Balloon (IAB) Catheter with a Fiber Optic Sensor and a Measurement System, 30cc Arrow Intra-Aortic Balloon (IAB) Catheter with a Fiber Optic Sensor and a Measurement System...
Health Headlines - January 29 by Meredy Registered NurseHealth Maven Cordis Recalls Balloon Catheters A problem that could cause injury or death has prompted Johnson & Johnson subsidiary Cordis to recall about 132,000 Dura Star RX and Fire Star RX PTCA balloon catheters...
Trick of the Trade: Foley balloon be gone! by Michelle Lin Medical Doctor of the catheter is the cause. How can you deflate the balloon so that the Foley catheter can be removed? Option 1 Cut the Foley catheter's balloon port. This should remove the one-way valve device...
Stent Catheter Recall-NanoCross Dilation Catheter Could Break During Use–Need Bar Code Technology to “Scan that Cath by Medical Quack Patient ExpertHealth Maven during use. Cracking or breaking of the catheter shaft may result in the inability to inflate or deflate the balloon..., there’s a ton of them.  Sure would be easier to scan that catheter with a bar code on the packaging...
Johnson & Johnson Acquiring Sinusitis Catheter Technology Company - Acclarent by Medical Quack Patient ExpertHealth Maven Product Launch From the Acclarent website: “The Balloon Sinuplasty™ System Using endoscopic techniques, the Balloon Sinuplasty™ system enables qualified otolaryngologists to dilate obstructed sinus...

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