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Other links at Articles > Business of Medicine |
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FDA Issues Class I Recall of LIFEPAK CR Plus Defibrillators
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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
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