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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, Software Versions B.05, B.06, B.06.5X, Model 867146 2 06/11/2018 FEI # 1218950
Philips Electronics North America Corporation
Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352 Exchange part (service numbe... 2 04/04/2017 FEI # 1218950
Philips Electronics North America Corporation
Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product Number: 865352 Exch... 2 10/20/2016 FEI # 1218950
Philips Electronics North America Corporation
Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping (2.4GHz) Product Number: 865... 2 10/20/2016 FEI # 1218950
Philips Electronics North America Corporation
Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping (1.4GHz) Product Numb... 2 10/20/2016 FEI # 1218950
Philips Electronics North America Corporation
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