ANDOVER, Mass., Oct. 3 (UPI) -- Philips says it is recalling some automated-external defibrillators due to a possible malfunction that could keep them from analyzing heart rhythms properly.
The HeartStart FR2+ models being recalled are M3860A and M3861A, distributed by Philips, and M3840A and M3841A, distributed by Laerdal Medical, the U.S. Food and Drug Administration said.
Philips recalls automated defibrillators - UPI.com