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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.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP60. Product Number: M8005A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP50. Product Number: M8004A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP40. Product Number: M8003A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP30. Product Number: M8002A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP20. Product Number: M8001A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP5. Product Number: M8105A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP2. Product Number: M8102A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
October 22, 2025Medical DevicesFDA
Philips North America recalls Cardiac Workstation 7000; Model Number: 860441;
Hazard: Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
October 22, 2025Medical DevicesFDA
Philips North America recalls Cardiac Workstation 5000; Model Number: 860439;
Hazard: Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324.
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311.
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Onco
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Sl
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
October 1, 2025Medical DevicesFDA
Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT
Hazard: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
August 6, 2025Medical DevicesFDA
Philips North America recalls Upgrade to MR 7700 Model Number (REF): 782130;
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 SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144;
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 SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
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 SmartPath to dStream for 3.0T Model Number (REF): 782145;
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 MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
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 MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152;
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 Intera 3.0T Quasar Dual Model Number (REF): 781150;
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 Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY);
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 Elition S Model Numbers (REF): (1) 781357, (2) 782106, (3) 782137, (4) 782150 (China ONLY);
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 Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
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 Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139;
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.