US FDA Slaps Another Class I Recall On Medtronic

The company’s Covidien catheters subject of latest recall

The US FDA has identified a recall of Covidien catheters due to a hub defect as class I. The agency’s most serious designation is yet another for the company, which has recently recalled several devices.

RECALL
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The Food and Drug Administration has hit Medtronic with yet another class I recall, this time for more than 1 million catheters under its Covidien subsidiary.

The company recalled nine dialysis catheters due to a hub defect, according to the FDA’s recall notice. The reason for the recall is the potential for the Palindrome and...

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