Every recall we track for Philips North America — 126 in all — plus the complaints and injury reports the public filed about them.
Philips recalls SmartPath to dStream 1.5T MRI systems with MR Elastography (MRE) due to potential stiffness value errors from image reconstruction settings. Affected units have specific model numbers and serial numbers.
Philips recalls SmartPath to dStream for XR and 3.0T MRI systems with MR Elastography (MRE) due to potential stiffness value errors in specific image reconstruction settings.
Philips recalls Ingenia Ambition X MRI scanners with MR Elastography (MRE) that may display incorrect stiffness values due to image reconstruction settings. Affected models include 781356, 782109, 782138, and 782160.
Philips recalls specific model numbers of their Upgrade to MR 7700 with MR Elastography (MRE) devices due to potential stiffness value errors in image reconstruction.
Philips recalls Ingenia Elition S MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from image reconstruction settings. Affected models include 781357, 782106, and 782137.
Philips recalls Evolution Upgrade 1.5T MRI scanners with MR Elastography (MRE) due to potential stiffness value errors causing inaccurate imaging. Affected models include 782116, 782148, and 782166.
Philips recalls Achieva 3.0T MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from specific image reconstruction settings. Affected units have model number 781278.
Philips recalls MR 7700 with MR Elastography (MRE) models 782120 and 782153 due to potential stiffness value errors in image reconstruction, which may lead to inaccurate scan results.
Philips recalls certain Ingenia 1.5T MRI machines with MR Elastography (MRE) due to potential stiffness value errors when specific image reconstruction parameters are used, which could lead to inaccurate scan results.
Philips recalls its Achieva 1.5T Initial system with MR Elastography (MRE) due to potential stiffness value errors from specific image reconstruction settings. Affected units have model number 781178.
Philips recalls Ingenia 3.0T CX MRI scanners with MR Elastography (MRE) due to potential stiffness value errors in image reconstruction, which could lead to inaccurate scan results.
Philips recalls Ingenia Elition X MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from specific image reconstruction parameters. Affected models include 781358, 782107, and 782136.
Philips recalls Ingenia 1.5T CX MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from image reconstruction settings. Affected units have model number 781262.
Philips recalls two model numbers of 1.5T MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from image reconstruction settings.
Philips recalls Ingenia Ambition S MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from specific image reconstruction settings. Affected models include 781359, 782108, and 782139.
Philips recalls Evolution 3.0T MRI with MR Elastography (MRE) models 782143 and 782162 due to potential stiffness value errors in image reconstruction.
Philips recalls Ingenia 3.0T MRI scanners with MR Elastography (MRE) that may display incorrect stiffness values due to image reconstruction settings.
Philips recalls SmartPath to Ingenia Elition X with MR Elastography (MRE) models 782118, 782144, and 782163 due to potential stiffness value errors in image reconstruction, which may lead to inaccurate scan results.
Philips recalls SmartPath to dStream 3.0T with MR Elastography (MRE) model 782145 due to potential stiffness value errors from image reconstruction settings. Affected units may display incorrect voxel sizes in scans.
Philips recalls Patient Information Center iX software version 4.5.0 due to upgrade notifications not informing users of changes. Affected units may require software updates to prevent unexpected system behavior.
Philips recalls Ingenia 1.5T MRI systems with specific software versions and product codes due to potential stiffness value errors in exported MR Elastography images. Affected units may show inaccurate stiffness maps when viewed in PACS systems.
Philips recalls certain MR 7700 systems with software versions R11.1 and R12.1 due to potential stiffness value errors in exported MRE stiffness maps. Affected units may need software updates to prevent inaccurate imaging results.
Philips recalls Ingenia Elition S MRI systems with specific software versions due to potential stiffness value errors in exported MRE reports. Affected units may show inaccurate stiffness maps when shared with PACS systems.
Philips recalls Ingenia Ambition X MRI systems with specific software versions due to potential stiffness value errors in exported MR Elastography images. Affected units may show inaccurate stiffness maps when shared with PACS systems.
Philips recalls specific MRI systems with software versions R11.1 and R12.1 due to potential stiffness value errors in exported MR Elastography scans. Affected units may need software updates to prevent inaccurate imaging results.
Philips recalls Evolution Upgrade 3.0T MRI systems with software versions R11.1 and R12.1 due to potential stiffness value errors in MRE reports. Affected units may need correction to ensure accurate medical imaging.
Philips recalls Ingenia Elition X MRI systems with specific software versions due to potential stiffness value errors in exported MRE stiffness maps. Affected units may show inaccurate results in medical imaging.
Philips recalls Ingenia 3.0T CX MRI systems with specific software versions due to potential stiffness value errors in exported MRE images. Affected units may show inaccurate stiffness maps when shared with PACS systems.
Philips recalls MR 7700 systems with specific software versions due to potential stiffness value errors in exported elastography maps. Affected units may show inaccurate medical imaging data.
Philips recalls Ingenia 3.0T MRI systems with specific software versions and product codes due to potential stiffness value errors in exported MR Elastography images.
Philips recalls certain Evolution Upgrade 1.5T MRI systems with specific software versions due to potential stiffness value errors in exported MR Elastography reports. Affected units may require correction to ensure accurate medical imaging results.
Philips recalls Ingenia Ambition S MRI systems with specific software versions due to potential stiffness value errors in exported elastography reports. Affected units may show inaccurate stiffness measurements in medical imaging.
Philips recalls SmartPath to dStream 3.0T MRI systems with software versions R11.1 and R12.1 due to potential stiffness value errors in MR Elastography images. Affected units may show inaccurate stiffness maps when viewed in PACS.
Philips recalls Azurion R3.0 interventional fluoroscopy systems (model 722234) shipped between July 2024 and June 2025 due to missing SSD spacer, which could fail FDA safety requirements for source-skin distance.
Philips recalls Cardiac Workstation 7000 model 860441 due to power short risk from a pinched wire. Affected units may cause electrical issues.
Philips recalls Cardiac Workstation 5000 model 860439 due to power module wire failure causing short circuits. Affected units may have short circuits that could lead to equipment malfunction.
Philips recalls Ingenia Ambition X MRI scanners with specific model numbers due to potential fire from gradient coil component failures. Affected units may produce smoke or fire if the coil overheats.
Philips recalls specific MRI scanners (model numbers 782120, 782153) due to potential fire risk from gradient coil failures. Affected units may produce smoke or fire if components overheat.
Philips recalls SmartPath to dStream MRI systems with specific model numbers due to potential fire risk from gradient coil component failures.
Philips recalls Ingenia 1.5T MRI systems with specific model numbers due to potential fire risk from gradient coil component failures. Affected units may produce smoke or fire. Consumers should check their model numbers against the list provided.
Philips recalls Intera 3.0T Quasar Dual MRI systems with model number 781150 due to potential fire risk from gradient coil failures. Affected units may produce smoke or fire.
Philips recalls Evolution Upgrade 1.5T MRI systems with specific model numbers due to risk of smoke or fire from gradient coil component failures. Affected units include model numbers 782116 and 782148.
Philips recalls Evolution Upgrade 3.0T MRI systems with model numbers 782117 and 782143 due to potential fire risk from gradient coil failures. Affected units may produce smoke or fire.
Philips recalls SmartPath to Ingenia Elition X MRI systems with model numbers 782118 and 782144 due to potential fire risk from gradient coil component failures. Affected units may produce smoke or fire.
Philips recalls Achieva XR MRI systems with specific model numbers due to potential fire risk from gradient coil component failures. Affected units may produce smoke or fire.
Philips recalls specific Ingenia Elition S MRI models (China only) due to potential fire risk from gradient coil component failures. Affected units may produce smoke or fire.
Philips recalls Ingenia 3.0T CX MRI systems with specific model numbers due to potential fire risk from gradient coil component failures. Affected units may produce smoke or fire.
Philips recalls 7700 MRI systems with model number 782130 due to gradient coil component failures that could produce smoke or fire. Affected units include specific serial numbers listed in the recall notice.
Philips recalls Achieva 3.0T MRI systems with specific model numbers due to potential fire risk from gradient coil failures. Affected units may produce smoke or fire if components fail.
Philips recalls certain Ingenia Ambition S MRI scanners (model numbers 781359, 782108, 782133, 782139) due to potential fire risk from gradient coil component failures.
Philips recalls specific MRI scanner models (MR 5300) due to potential fire risk from gradient coil component failures. Affected units include certain model numbers sold in China. No remedy is provided in the recall notice.
Philips recalls Ingenia 3.0T MRI systems with model numbers 781342, 781377, 782103 for potential gradient coil component failures that could cause smoke or fire.
Philips recalls Ingenia 1.5T S MRI systems with model number 781347 due to potential gradient coil failures that could cause smoke or fire. Affected units include specific serial numbers listed in the recall notice.
Philips recalls SmartPath to dStream 3.0T MRI systems with model 782145 due to potential fire risk from gradient coil failures. Affected units may produce smoke or fire.
Philips recalls Ingenia Elition X MRI scanners with specific model numbers (China only) due to potential fire from gradient coil failures. Affected units may produce smoke or fire.
Philips recalls Achieva XR MRI scanners with specific product numbers due to a gradient coil component that may overheat, causing smoke or fire. This poses risks of injury or death to patients and staff if smoke or fire occurs.
Philips recalls Intera 1.5T Omni/Stellar MRI systems with specific serial numbers due to potential fire risk from gradient coil component failure. Affected units may produce smoke or fire, risking injury or death to patients and staff.
Philips recalls Intera 1.5T Master/Nova MRI systems with Product Number 781106 due to potential fire risk from Gradient Coil component failure. Affected units may produce smoke or fire, risking injury or death.
Philips recalls Intera Achieva 1.5T Pulsar MRI systems with specific serial numbers due to a potential fire risk from gradient coil failure. Affected units may produce smoke or fire, risking injury or death to patients and staff.
Philips recalls Intera 1.5T Achieva Nova MRI systems with specific serial numbers due to potential fire and smoke risks from gradient coil failures. Affected units may cause injury or death if smoke or fire occurs.
