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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K113125
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Product Description
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FDA Recall
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IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countries: 453564... 2 06/01/2019 FEI # 1218950
Philips North America, LLC
IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262... 2 06/01/2019 FEI # 1218950
Philips North America, LLC
IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 45356... 2 06/01/2019 FEI # 1218950
Philips North America, LLC
IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06... 2 05/21/2021 FEI # 3016618143
Philips North America Llc
Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Produc... 2 10/08/2024 FEI # 3006648320
Philips North America
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