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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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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2144-2018 - IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 867146 2 06/11/2018 Philips Electronics North America Corporation
Z-2143-2018 - IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865352 2 06/11/2018 Philips Electronics North America Corporation
Z-2142-2018 - IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865351 2 06/11/2018 Philips Electronics North America Corporation
Z-2141-2018 - IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350 2 06/11/2018 Philips Electronics North America Corporation
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