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Home » FDA Updates Medtronic Hemodialysis Catheters Recall to Class I
FDA Updates Medtronic Hemodialysis Catheters Recall to Class I
The FDA has updated Medtronic’s November 2022 recall of its Mahurkar Acute Dual Lumen High Flow (13.5 French) hemodialysis catheters to Class I, due to a potential catheter hub defect that could cause the catheter tubes to leak, possibly leading to serious injury or death.