Risk Of Cardiac Arrest Leads To Recall Of Medtronic ICDs

Medtronic has recalled hundreds of thousands of ICDs citing a shock risk that could cause cardiac arrest. The FDA has given the recall its most serious classification.

HeartBeat
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The US Food and Drug Administration has designated a recall from Medtronic as class I, its most serious type.

The company initiated the recall of nearly 350,000 implantable defibrillators in May because the devices may deliver a reduced energy...

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