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Hidden Reports Masked The Scope Of Widespread Harm From Faulty Heart Device

Faced with the possibility that a bout of abnormal heartbeats could end his life, in 2006, Dr. Marc Sicklick had a small device implanted in his chest that would shock it back into rhythm. Soon he would struggle with another life-or-death choice: whether to remove the Sprint Fidelis, which was deemed dangerous and recalled in 2007 after it had been implanted in hundreds of thousands of patients. The Sprint Fidelis was prone to giving patients random electrical jolts — and sometimes failed to fire in genuine cardiac emergencies, according to manufacturer Medtronic’s letter to doctors. What Sicklick and thousands of others in his position have not known is that the Food and Drug Adm...

Read the full post at Syndicate – Kaiser Health News
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