The U.S. Food and Drug administration has ordered St. Jude Medical to do additional studies on patients implanted with medical device components that are blamed in as many as 20 deaths.
According to the New York Times, the FDA has also recommended that patients who received the Riata defibrillator lead — a wire that connects a defibrillator to a patient’s heart — get X-rays or other imaging to check for problems.
The ...
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