The U.S. FDA posted notice of a class I recall for two hemodialysis catheters made by Covidien Inc., the Palindrome and Mahurkar catheters, due to a catheter hub defect that could lead to mixing of ...

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Medtronic has asked healthcare providers to immediately stop using more than 1 million catheters distributed across the U.S. and around the world after discovering a potential safety risk within the ...

Medtronic has recalled more than 1 million catheters used for hemodialysis, which filters waste, salt and fluid from a patient's blood. Last week the FDA labeled the action a Class 1 recall, the ...

Minneapolis-based Medtronic has recalled Palindrome and Mahurkar hemodialysis catheters, which the FDA deemed a class 1 recall, the highest level. The recall is due to a catheter hub defect that could ...