On January 20, 2023, the U.S. Food and Drug Administration (FDA) announced that Medtronic would recall more than 22,000 hemodialysis catheters. The Class I recall, the most severe type of product recall, of the Mahurkar Acute Dual Lumen High Flow (13.5 French) Hemodialysis Catheters followed reports of two injuries. Medtronic … [Read more...] about Covidien Palindrome and Mahurkar Hemodialysis Catheter Recalls