230,000 Medical Device Adverse Events Reported to FDA in 2010

Of the more than 230,000 medical device-related adverse events reported to the Food and Drug Administration in 2010, approximately 30,000 yielded “very serious” outcomes such as hospitalization or death, according to research conducted by Clarimed.

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By: Staff

Read the full report in Becker’s ASC Review on medical device-related adverse events.

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