Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K113125 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 865350, Service # USA: 453564262491 and 453564262511... | 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 |
| IntelliVue MX40 Patient Monitor, Model Nos. 865350, 865351, 865352, 867146 - Product Usage: Indicate... | 2 | 12/10/2018 |
FEI # 1218950 Philips Electronics North America Corporation |
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