Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 |
FEI # 1000127138 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 |
FEI # 1000127138 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 |
FEI # 1000127138 Lifewatch Services Inc |
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