SILVER SPRING, Md., May 6 The Food and Drug Administration (FDA) has alerted the public about the following products.
These alerts were prompted by reports that FDA received from health care professionals and patients through the agency's MedWatch Adverse Event Reporting Program.
Read more about these safety alerts and what to do if you've used one of the affected products at http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm210794.htm
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CONTACT: Jason Brodsky, +1-301-796-8234, [email protected]
-- Certain external defibrillators that were recalled because they may malfunction during attempts to rescue people in sudden cardiac arrest
SOURCE U.S. Food and Drug Administration