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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K021453
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FDA Recall
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Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are an accessory to the compa... 2 05/27/2020 FEI # 1218950
Philips North America, LLC
Philips HeartStart XL M4735A Defibrillator/Monitors, used with the M3516A batteries The Heart St... 2 10/04/2012 FEI # 1218950
Philips Healthcare Inc.
HeartStart XL Model M4735A Defibrillator, Automatic, External Defibrillator-Monitor. The defibr... 2 05/19/2009 FEI # 1218950
Philips Healthcare Inc.
HeartStart XL Defibrillator/Monitor, Model: M4735A 2 10/25/2007 FEI # 1218950
Philips Medical Systems
Philips Medical HeartStartXL Defibrillator/Monitor Model : M4735A 2 08/07/2007 FEI # 1218950
Philips Medical Systems
Model M4735A HeartStart XL Defibrillator//Monitor 2 09/11/2003 FEI # 1218950
Philips Medical Systems
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