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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2508-2024 - IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866060. Indicated for use by health care professionals for monitoring and recording of, and to g... 2 08/05/2024 Philips North America Llc
Z-2511-2024 - IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866066. Indicated for use by health care professionals for monitoring and recording of, and to g... 2 08/05/2024 Philips North America Llc
Z-2510-2024 - IntelliVue Patient Monitor MX500 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866064. Indicated for use by health care professionals for monitoring and recording of, and to g... 2 08/05/2024 Philips North America Llc
Z-2509-2024 - IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866062. Indicated for use by health care professionals for monitoring and recording of, and to ... 2 08/05/2024 Philips North America Llc
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