Medtronic Expands Previous Recall on Hemodialysis Catheters Due to Potential for Leakage
The U.S. Food and Drug Administration (FDA) recently announced the recall of over 22,000 Medtronic Mahurkar Acute Lumen High Flow Hemodialysis Catheters because the devices may cause serious injuries or death. These catheters are implanted under the skin for up to three weeks to filter…