# China NMPA Product Recall - Digital Medical X-ray Radiography System, Medical Diagnostic X-ray System, Fluoroscopy Radiography X-ray Equipment

Source: https://www.globalkeysolutions.net/records/china_product_recall/philips-medical-systems/a62f7aec-0d77-400d-ba3c-cc6462ed7eac/
Source feed: China

> China NMPA product recall for Digital Medical X-ray Radiography System, Medical Diagnostic X-ray System, Fluoroscopy Radiography X-ray Equipment by Philips Medical Systems published December 19, 2025. Recall level: . Philips Medical Systems DMC GmbH, with its affiliate Philips (China) Investment Co., Ltd. reporting,

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Philips Medical Systems DMC GmbH is voluntarily recalling its Digital Media X-ray Radiography System, Medical Diagnostic X-ray System, and Fluoroscopy Radiography X-ray Equipment.
- Company Name: Philips Medical Systems
- Publication Date: 2025-12-19
- Product Name: Digital Medical X-ray Radiography System, Medical Diagnostic X-ray System, Fluoroscopy Radiography X-ray Equipment
- Recall Reason: Some Philips X-ray diagnostic system (DXR) ceiling-mounted telescopic brackets manufactured between July 2024 and June 2025 may have quality issues, potentially requiring greater force or physical exertion for manual movement.
- Discovering Company: Philips (China) Investment Co., Ltd.
- Manufacturing Company: Philips Medical Systems
- Summary: Philips Medical Systems DMC GmbH, with its affiliate Philips (China) Investment Co., Ltd. reporting, has initiated a voluntary recall of several X-ray diagnostic systems. The affected products include the Medical Diagnostic X-ray System, Fluoroscopy Radiography X-ray Equipment, and Digital Media X-ray Radiography System. This recall is prompted by potential quality issues identified in the ceiling-mounted telescopic brackets of units manufactured between July 2024 and June 2025. These issues may necessitate increased physical exertion to manually move the equipment, posing a potential operational inconvenience. The action is being taken under the regulatory oversight of the National Medical Products Administration (NMPA) of China. As a required action, the company is voluntarily recalling the affected devices to address and resolve these quality concerns.

Company: https://www.globalkeysolutions.net/companies/philips-medical-systems/91e33b43-88a2-4a53-9bcd-1d32f1abde47/