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Philips North America Recalls
530 recalls on record · April 5, 2017 to July 1, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 6, 2025Medical DevicesFDA
Philips North America recalls Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Ingenia 1.5T S Model Number (REF): 781347;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116, (2) 782148;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Achieva XR; Model Numbers (REF): (1) 781153, (2) 781253;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
August 6, 2025Medical DevicesFDA
Philips North America recalls Achieva 3.0T; Model Numbers (REF): (1) 781177, (2) 781277, (3) 781278, (4) 781344, (5) 781345;
Hazard: The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
July 2, 2025Medical DevicesFDA
Philips North America Llc recalls Spectral CT. Computed tomography X-ray system.
Hazard: Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software issues that affect CT performance.
June 18, 2025Medical DevicesFDA
Philips North America recalls SmartPath to dStream for 1.5T¿; Product Number: 782146;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera Achieva 1.5T Pulsar; Product Number: 781171;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera 1.5T Omni/Stellar; Product Number: 781104;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera 1.5T Master/Nova Product Number: 781106;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera 1.5T Explorer/Nova Dual Product Number: 781108;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera 1.5T Achieva Nova-Dual Product Number: 781173;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera 1.5T Achieva Nova Product Number: 781172;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Intera 1.5T Achieva IT Nova Product Number: 781175
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
June 18, 2025Medical DevicesFDA
Philips North America recalls Achieva XR Product Numbers: (1) 781153, (2) 781253;
Hazard: identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia 3.0T CX; Model Number: 781271;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia 1.5T CX; Model Number: 781262;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia 1.5T S; Model Number: 781347;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
May 28, 2025Medical DevicesFDA
Philips North America Llc recalls Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Hazard: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.