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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K013425
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FDA Recall
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HeartStart FR2+ AED with ECG Display, Model M3860, Philips brand, configurable manual charge in adva... 2 11/29/2010 Philips Medical Systems
HeartStart FR2+ AED with ECG Display, Model 989803148601. This product is G2005 Update according t... 2 11/29/2010 Philips Medical Systems
HeartStart FR2+ AED with Text Display (No ECG), Model 3841, Laerdal brand, no configurable manual ch... 2 11/29/2010 Philips Medical Systems
HeartStart FR2+ AED with ECG Display, Model 3840, Laerdal brand, configurable manual charge in advan... 2 11/29/2010 Philips Medical Systems
HeartStart FR2+ AED with Text Display, Model 989803148611. This product is G2005 Update in accorda... 2 11/29/2010 Philips Medical Systems
HeartStart FR2+ AED with Text Display (No ECG), Model M3861, Philips brand, no configurable manual c... 2 11/29/2010 Philips Medical Systems
HeartStart FR2+ automated external defibrillator (AED) model: M3841: LAERDAL brand; text prompts onl... 2 11/26/2010 Philips Medical Systems
HeartStart FR2+ automated external defibrillator (AED) model: M3861: PHILIPS brand; text prompts o... 2 11/26/2010 Philips Medical Systems
HeartStart FR2+ automated external defibrillator (AED) model: M3840: LAERDAL brand; configurable ... 2 11/26/2010 Philips Medical Systems
HeartStart FR2+ automated external defibrillator (AED) Model M3860: Philips brand; configurable ECG ... 2 11/26/2010 Philips Medical Systems
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