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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0856-2016 - Philips Healthcare IntelliVue Info Center iX, A.0 866023 2 02/23/2016 Philips Electronics North America Corporation
Z-0858-2016 - Philips Healthcare IntelliVue Info Center iX, B.0, 866389 Physiological, Patient Monitor (With Arrhythmia Detection or Alarm) 2 02/23/2016 Philips Electronics North America Corporation
Z-0857-2016 - Philips Healthcare PIIC Classic Upgrade, 866117 Physiological, Patient Monitor (With Arrhythmia Detection or Alarm) 2 02/23/2016 Philips Electronics North America Corporation
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