FDA Issues Class I Recall for Teleflex Catheter System: Potential for Serious Injury and Blockage Introduction: The US Food and Drug Administration (FDA) has issued a Class I recall for more than 260,000 catheter systems manufactured by Teleflex, specifically its subsidiary Arrow International. The recall was initiated due to … [Read more...] about Teleflex Arrow Endurance Dwell Peripheral Catheter System Lawsuit Attorneys