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Automated external defibrillators (AEDs), which are used to resuscitate victims of sudden cardiac arrest, are not adequately tracked and have a greater than 20 percent chance of being recalled, according to a new study.
The FDA has posted a Class I recall of Welch Allyn’s AED 20 automated external defibrillators manufactured by MRL from April through October 2003. The company isssued the recall June 15.