Every recall we track for Philips Healthcare — 11 in all — plus the complaints and injury reports the public filed about them.
Philips Healthcare recalls Incisive CT software version 5.0 due to potential scan inaccuracies that could affect medical imaging results. Affected units may require software updates to ensure proper scan planning and safety.
Philips recalls StentBoost Live R2.0 software for Azurion systems with R2.x software due to incorrect EPX database configuration causing acquisition to continue after 40 images instead of stopping automatically.
Philips recalls Azurion systems with specific software versions due to potential 3D X-ray scan errors. Affected units may produce inaccurate scans if detector orientation is not precisely aligned.
Philips Healthcare recalls ProxiDiagnost N90 multi-functional R/F systems due to missing required radiation labels, which could lead to improper radiation exposure. Affected units may need label verification.
Philips Healthcare recalls DigitalDiagnost C9: Some units lack required radiation labels, posing risks for medical use. Check if your device has missing labels and contact Philips for details.
Philips Healthcare recalls CombiDiagnost R90 medical devices due to missing required radiation labels, which could affect safety compliance. Affected units may need verification of labels.
Philips Healthcare recalls Azurion systems with software release R2.0.x due to a defect causing incorrect patient type selection during studies, potentially affecting dose control. Affected units include Azurion R2.1 models.
Philips recalls DigitalDiagnost C50 X-ray systems due to a missing label. This may affect safety and compliance. Contact Philips for details.
Philips Healthcare recalls Allura Xper imaging systems for vascular and cardiac procedures due to shutter reset risk when changing procedure types during a single exam. Affected models include Allura 8.1.25 and 8.2.25 series. No immediate action required but check for specific model numbers.
Philips Healthcare recalls UNIQ products for vascular and cardiovascular imaging where shutter positions reset during procedure changes, potentially affecting patient safety. Learn if your device is affected and what to do.
Philips Healthcare recalls Centron imaging products for potential shutter reset during procedure changes, affecting vascular and cardiac imaging. Users should check model numbers and contact Philips for guidance.
