Philips Medical Systems Recalls

3 recalls found for Philips Medical Systems. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Imaging Systems Over Malfunction Risk

Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane systems on September 3, 2025. The recall affects units distributed globally due to potential failures in internal components. If malfunction occurs, motorized movements will be disabled, posing risks to operational efficiency.

Philips Medical Systems
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Imaging Systems Due to Malfunction Risk

Philips Medical Systems recalled 2,114 Allura Xper FD20 imaging systems on September 3, 2025. The systems may fail due to internal component deterioration, risking loss of motorized functionality. This recall affects 791 units in the U.S. and 1,323 globally.

Philips Medical Systems
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Radiation Therapy Planning Software

Philips Medical Systems recalled 810 units of its Radiation Therapy Planning System on August 5, 2025. A software issue may cause image errors during treatment planning. Affected models include Pinnacle TumorLOC and Multimodality Simulation Workspace.

Philips Medical Systems
Due to
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Brand Statistics

Total Recalls
3
Pages
1