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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0206-2012 - LifeStar ACT I Sensor Ambulatory Cardiac Telemetry; an automatically activated system with a single channel EKG, office hookup and auto send/auto detect that requires no patient intervention to either... 2 11/17/2011 Lifewatch Services Inc
Z-0208-2012 - ACT Cellular Phone Monitor; a component of the ACT Ambulatory Cardiac Telemetry; an automatically activated system with a high performance EKG, office hookup and auto send/auto detect that requires no... 2 11/17/2011 Lifewatch Services Inc
Z-0207-2012 - LifeStar ACT III Platinum Sensor Ambulatory Cardiac Telemetry; an automatically activated system with a high performance triple channel EKG, office hookup and auto send/auto detect that requires no pa... 2 11/17/2011 Lifewatch Services Inc
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