News | News By Subject | News by Disease News By Date | Search News
Get Our FREE
Industry eNewsletter
email:    
   

FDA Designates AngioScore, Inc.'s Angiosculpt Balloon Catheters Recall As Class 1


9/9/2010 9:14:57 AM

News Inferno -- AngioScore Inc.’s AngioSculpt’s EX Percutaneous Transluminal Coronary Angioplasty (PTCA) scoring balloon catheters are subject to a Class I recall. According to the recall notice, the catheters may fragment and become lodged in a patient’s coronary arteries, resulting in serious injuries and even death.

Read at News Release
Read at News Release


comments powered by Disqus
   

ADD TO DEL.ICIO.US    ADD TO DIGG    ADD TO FURL    ADD TO STUMBLEUPON    ADD TO TECHNORATI FAVORITES