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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K202564
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DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. 2 06/05/2026 FEI # 3016618143
Philips North America Llc
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital... 2 11/08/2023 FEI # 3016618143
Philips North America Llc
DigitalDiagnost C90 High Performance, used to acquire, process, store, display and export digital ra... 2 11/08/2023 FEI # 3016618143
Philips North America Llc
DigitalDiagnost C90, Model No. 712034 and 712035 2 06/30/2023 FEI # 3016618143
Philips North America Llc
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 71... 2 11/07/2025 FEI # 3003768251
Philips Medical Systems DMC GmbH
DigitalDiagnost C90 High Performance. radiography and fluoroscopy system 2 07/12/2022 FEI # 3003768251
Philips Medical Systems DMC GmbH
DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system 2 07/12/2022 FEI # 3003768251
Philips Medical Systems DMC GmbH
DigitalDiagnost C90 2 11/24/2021 FEI # 1218950
Philips Healthcare
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