Medical Device Recalls
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1 to 10 of 22 Results
510(K) Number: K160743 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2.... | 2 | 09/19/2025 |
FEI # 3016618143 Philips North America Llc |
| Model 728321/728323 CT5000 Ingenuity Plus/Pro/Premium-Computed Tomography X-ray system | 2 | 08/18/2021 |
FEI # 3016618143 Philips North America Llc |
| 728327 Ingenuity CT Upgrades-Computed Tomography X-ray system | 2 | 08/18/2021 |
FEI # 3016618143 Philips North America Llc |
| Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Ingenuity Core, Ingenui... | 2 | 06/30/2021 |
FEI # 3016618143 Philips North America Llc |
| Ingenuity CT, Model # 728326, computed tomography x-ray system | 2 | 08/06/2019 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| Ingenuity Core Model # 728321, computed tomography x-ray system | 2 | 08/06/2019 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| Ingenuity Core128 Model # 728323, computed tomography x-ray system | 2 | 08/06/2019 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| Ingenuity Core128/Elite China 728324 | 2 | 06/22/2018 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| Ingenuity Core128 728323 | 2 | 06/22/2018 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| Philips Ingenuity Core 728321 | 2 | 06/22/2018 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
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