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Philips Medical Systems DMC GmbH FDA Recalls
11 recalls on file across devices, 0 of them Class I and 11 still open. This firm is not matched to a listed company.
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Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| Radiography 7300 C; Model Number: 712037;Class IIOct 1, 2025Philips has identified that some ceiling suspension telescop |
| Precision CRF; Model Number: 706400;Class IIOct 1, 2025Philips has identified that some ceiling suspension telescop |
| ProxiDiagnost N90; Model Number: 706110;Class IIOct 1, 2025Philips has identified that some ceiling suspension telescop |
| DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;Class IIOct 1, 2025Philips has identified that some ceiling suspension telescop |
| CombiDiagnost R90; Model Number: 709031;Class IIOct 1, 2025Philips has identified that some ceiling suspension telescop |
| DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;Class IIOct 1, 2025Philips has identified that some ceiling suspension telescop |
| ProxiDiagnost N90. radiography and fluoroscopy systemClass IIMay 19, 2021Following a system restart where the Table Height 2 (TH2) is |
| DigitalDiagnost C90 High Performance. radiography and fluoroscopy systemClass IIMay 19, 2021Following a system restart where the Table Height 2 (TH2) is |
| DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy systemClass IIMay 19, 2021Following a system restart where the Table Height 2 (TH2) is |
| DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy systemClass IIMay 19, 2021Following a system restart where the Table Height 2 (TH2) is |
| DigitalDiagnost 4 High Performance. radiography and fluoroscopy systemClass IIMay 19, 2021Following a system restart where the Table Height 2 (TH2) is |