Medtronic Plc
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FDA Says Medtronic Recalls Mahurkar Acute Dual Lumen High Flow Hemodialysis Catheters For Potential Catheter Hub Defect
Published: 01/30/2023 17:15 GMT
Medtronic Plc (MDT) - :fda - Medtronic Recalls Mahurkar Acute Dual Lumen High Flow Hemodialysis Catheters for Potential Catheter Hub Defect.
FDA - Identified Mahurkar Acute Dual Lumen High Flow (13.5 French) Hemodialysis Catheters Recall As a Class I Recall.
FDA - There Have Been Two Injuries Reported Related to Use of Medtronic's Defective Catheter and No Reports of Death.
FDA - Identified Mahurkar Acute Dual Lumen High Flow (13.5 French) Hemodialysis Catheters Recall As a Class I Recall.
FDA - There Have Been Two Injuries Reported Related to Use of Medtronic's Defective Catheter and No Reports of Death.