| Subject: | FDA Issues Class I Recall of NexStent Monorail, NexStent Carotid Stent and Monorail Delivery System |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 14 Aug 2008 - 02:00 pm |
| The Food and Drug Administration (FDA) and Boston Scientific are informing healthcare professionals and patients of the Class I Recall of NexStent Monorail, NexStent Carotid Stent and Monorail Delivery System, distributed from June 19, 2007, through May 5, 2008. The device is used in patients to treat a blockage in carotid artery disease. The product was recalled because the tip of the stent delivery system may detach during a carotid artery stenting procedure. This could lead to increased... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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