| Subject: | FDA Announces Class I Recall for Arrow International 30cc, 40cc and 50cc Intra Aortic Balloon Pump (IAB) Catheters |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 15 Apr 2009 - 05:00 pm |
| The Food and Drug Administration (FDA) and Teleflex Medical have notified healthcare professionals of the Class I Recall for Arrow International 30cc, 40cc and 50cc Intra Aortic Balloon Pump (IAB) Catheters, a component of the Intra-Aortic Pump System which is designed to provide cardiac assist therapy to increase blood flow to the heart. Please see the FDA's Recall Notice, a link to which is provided below, for a list of the specific models recalled. This Recall is being conducted... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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