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Home » Makers of AEDs: Increase in MDRs Due to the FDA’s Reporting Policy
Makers of AEDs: Increase in MDRs Due to the FDA’s Reporting Policy
December 17, 2010
An increase in serious adverse events tied to automatic external defibrillators (AEDs) may have less to do with faulty manufacturing issues than with industry confusion over the FDA’s medical device reporting (MDR) policy.