Every recall we track for Philips Medical Systems DMC GmbH — 11 in all — plus the complaints and injury reports the public filed about them.
Philips recalls DigitalDiagnost 4 (High Performance and Flex/Value models) manufactured July 2024-June 2025 due to potential difficulty moving the telescopic carriage, requiring extra force. Affected units have specific model numbers and serials.
Philips recalls CombiDiagnost R90 model 709031 produced July 2024-June 2025 due to potential difficulty moving ceiling suspension telescopic carriages requiring extra force. Affected units may need special handling.
Philips recalls some ProxiDiagnost N90 ceiling suspension telescopic carriages (model 706110) manufactured July 2024-June 2025 that may require more physical effort to move vertically due to manufacturing issues.
Philips recalls Precision CRF ceiling suspension telescopic carriages (model 706400) made between July 2024 and June 2025 that may require extra force to move vertically due to manufacturing issues. Affected units can be identified by serial numbers starting with 19-40.
Philips recalls DigitalDiagnost C90 models (712034/712035) produced July 2024-June 2025 that may be difficult to move vertically due to manufacturing issues. Consumers should check serial numbers for affected units.
Philips recalls Radiography 7300 C models from July 2024 to June 2025 that may require extra force to move vertically due to manufacturing issues. Affected units have specific serial numbers and model numbers.
Philips recalls DigitalDiagnost 4 Flex/Value radiography systems with specific serial numbers due to potential incorrect radiation dose from misaligned image fields after system restarts. Affected units may show wrong anatomy positioning during exams.
Philips recalls DigitalDiagnost C90 radiography systems due to incorrect radiation dose and image orientation risks after system restarts with Wallstand VS2. Affected units may require correction to prevent misdiagnosis.
Philips recalls DigitalDiagnost C90 radiography systems with serial numbers starting 10001073-10001201 and others. Incorrect radiation dose and image orientation may occur after system restarts using Wallstand VS2, requiring immediate attention.
Philips recalls ProxiDiagnost N90 radiography systems with serial numbers 10001002-10001064. Incorrect radiation dose and misaligned anatomy markers may occur due to firmware issues after system restarts.
Philips recalls DigitalDiagnost 4 High Performance radiography systems with incorrect radiation dose risk after system restarts. Affected units may show wrong image orientation and misaligned anatomical markers.
