Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K122439 |
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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 MP20. Product Number: M8001A. | 2 | 12/02/2025 |
FEI # 3016618143 Philips North America Llc |
| IntelliVue MP30. Product Number: M8002A. | 2 | 12/02/2025 |
FEI # 3016618143 Philips North America Llc |
| NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383) | 2 | 05/31/2017 |
FEI # 1218950 Philips Electronics North America Corporation |
| Philips IntelliVue Monitors with software revisions J.21.03, J.21.19. Model Product MP5 M810... | 2 | 10/21/2014 |
FEI # 1218950 Philips Medical Systems, Inc. |
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