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FDA Issues Class I Recall of LIFEPAK CR Plus Defibrillators
Link ID 18579
Title FDA Issues Class I Recall of LIFEPAK CR Plus Defibrillators
Url http://www.medscape.com/viewarticle/709045?src=rss
Description The Food and Drug Administration issued a class I recall of the LIFEPAK CR Plus automated external defibrillators (Physio-Control, Redmond, WA) [1]. The recall affects models manufactured and distributed from July 9, 2008 through August 19, 2008. Heartwire
Category Articles > Business of Medicine
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Date Sep 17, 2009
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