Philips Medical Systems Netherlands B.V. Recalls

2 recalls found for Philips Medical Systems Netherlands B.V.. Check if any of your products are affected.

HIGHFDA DEVICE

Philips Medical Systems Recalls Operating Room Table Over Hazard

Philips Medical Systems Netherlands B.V. recalled three Allura Xper FD20/20 OR Tables on September 3, 2025. The recall addresses potential failures in internal components that could impede motorized functions. Users must stop using the device immediately and follow recall instructions.

Philips Medical Systems Netherlands B.V.
Systems may
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HIGHFDA DEVICE

Philips Medical Systems Recalls X-ray Imaging Systems Due to Malfunction Risk

Philips Medical Systems Netherlands B.V. recalled 1,117 X-ray imaging systems on September 3, 2025. The recall affects product codes 722010, 722026, and 722003 due to potential internal component deterioration. This issue may render motorized movements inoperable, posing a risk to patient care.

Philips Medical Systems Netherlands B.V.
Systems may
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Brand Statistics

Total Recalls
2
Pages
1