Philips North America Llc recalls

98 recalls on record · latest: January 7, 2026

Official U.S. recall history for Philips North America Llc, compiled from official government records.

Get recall alerts

Free email alert whenever Philips North America Llc has a new recall — straight from official government data. Unsubscribe anytime.

Philips North America Llc recalls Spectral CT 7500 on Rails; Product Code (REF): 728334;

January 7, 2026 · Medical device recalls Moderate risk As part of the CT systems sub assembly, thirty-two (32) fasteners are used to a…

Philips North America Llc recalls IQon Spectral CT; Product Code (REF): 728332;

January 7, 2026 · Medical device recalls Moderate risk As part of the CT systems sub assembly, thirty-two (32) fasteners are used to a…

Philips North America Llc recalls Spectral CT; Product Code (REF): 728333;

January 7, 2026 · Medical device recalls Moderate risk As part of the CT systems sub assembly, thirty-two (32) fasteners are used to a…

Philips North America Llc recalls Brilliance iCT; Product Code (REF): 728306;

January 7, 2026 · Medical device recalls Moderate risk As part of the CT systems sub assembly, thirty-two (32) fasteners are used to a…

Philips North America Llc recalls Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.

December 12, 2025 · Medical device recalls Moderate risk It was found that the MX40 device could not reconnect to the PIC iX when moving…

Philips North America Llc recalls IntelliVue MP70. Product Number: M8007A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX450. Product Number: 866062.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX750. Product Number: 866471.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX550. Product Number: 866066.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Multi-Measurement Module X3. Product Number: 867030.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX400. Product Number: 866060.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX600. Product Number: 865242.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP20. Product Number: M8001A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP5. Product Number: M8105A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP60. Product Number: M8005A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Multi Measurement Server X2. Product Number: M3002A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP40. Product Number: M8003A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX100. Product Number: 867033.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP80. Product Number: M8008A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP50. Product Number: M8004A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP2. Product Number: M8102A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX850. Product Number: 866470.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX500. Product Number: 866064.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX700. Product Number: 865241.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue Patient Monitor MX800. Product Number: 865240.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP30. Product Number: M8002A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls IntelliVue MP90. Product Number: M8010A.

October 31, 2025 · Medical device recalls Moderate risk Potential issue where the IntelliVue monitors did not alarm.

Philips North America Llc recalls Incisive CT; Software Version Number: 4.5, 5.0, 5.1;

October 29, 2025 · Medical device recalls Moderate risk If the screws of tube heat exchanger on the rotating scanner are not tightened…

Philips North America Llc recalls CT 5300; Software Version Number: 4.5, 5.0, 5.1;

October 29, 2025 · Medical device recalls Moderate risk If the screws of tube heat exchanger on the rotating scanner are not tightened…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311.

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324.

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Mode…

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Cha…

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, M…

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology,…

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.

August 13, 2025 · Medical device recalls Moderate risk The patient support table (couch) may descend unexpectedly to the lowermost pos…

Philips North America Llc recalls Spectral CT. Computed tomography X-ray system.

May 29, 2025 · Medical device recalls Moderate risk Devices with affected software may experience two unintended motion issues that…

Philips North America Llc recalls Product Name: Upgrade to MR 7700; Model Number: 782130;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: SmartPath to dStream for 3.0T; Model Number: 782145

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia 1.5T S; Model Number: 781347;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia 1.5T CX; Model Number: 781262;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Ingenia 3.0T CX; Model Number: 781271;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;

May 13, 2025 · Medical device recalls Moderate risk Potential for alignment errors in the cross reference line functionality when r…

Philips North America Llc recalls Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intu…

April 7, 2025 · Medical device recalls Moderate risk Disconnection of the adapter from the endotracheal tube can potentially be diff…

Philips North America Llc recalls Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.

April 1, 2025 · Medical device recalls Moderate risk Unintended motion issues related to Interventional Control that may lead to col…

Philips North America Llc recalls Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.

March 10, 2025 · Medical device recalls Moderate risk Potential for collimator to fall as a result of incorrect installation.

Philips North America Llc recalls Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.

March 10, 2025 · Medical device recalls Moderate risk Potential for collimator to fall as a result of incorrect installation.

Philips North America Llc recalls Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, i…

February 25, 2025 · Medical device recalls Moderate risk A wireless foot switch pedal may get stuck in the active position when the user…

Philips North America Llc recalls Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic…

February 25, 2025 · Medical device recalls Moderate risk A wireless foot switch pedal may get stuck in the active position when the user…

Philips North America Llc recalls Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization during diagnostic, i…

February 25, 2025 · Medical device recalls Moderate risk A wireless foot switch pedal may get stuck in the active position when the user…

Philips North America Llc recalls IntelliBridge EC10 Module. Model Number: 865115

January 15, 2025 · Medical device recalls Moderate risk Potential failure to alarm for "No Device Data" INOP. The device to alarm after…

Philips North America Llc recalls IntelliVue Patient Monitor MX500. Model Number: 866064

January 15, 2025 · Medical device recalls Moderate risk Potential failure to alarm for "No Device Data" INOP. The device to alarm after…

Philips North America Llc recalls IntelliVue Patient Monitor MX550. Model Number: 866066

January 15, 2025 · Medical device recalls Moderate risk Potential failure to alarm for "No Device Data" INOP. The device to alarm after…

Philips North America Llc recalls IntelliVue Patient Monitor MX450. Model Number: 866062

January 15, 2025 · Medical device recalls Moderate risk Potential failure to alarm for "No Device Data" INOP. The device to alarm after…

Philips North America Llc recalls IntelliVue Patient Monitor MX400. Model Number: 866060

January 15, 2025 · Medical device recalls Moderate risk Potential failure to alarm for "No Device Data" INOP. The device to alarm after…

Philips North America Llc recalls Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216

November 20, 2024 · Medical device recalls Moderate risk The following four issues are included: 1. Certain Channel Settings may result…

Philips North America Llc recalls Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.

November 16, 2024 · Medical device recalls Moderate risk Potential for a plan box not updated issue during Interventional procedure with…

Philips North America Llc recalls Achieva TX Interventional Coil 3.0T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls Mammotrak Diagnostic Coil 3.0T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls Mammotrak Interventional Coil 1.5T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls ST SENSE Breast Coil

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls dS Breast 16ch 3.0T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls dS Breast 7ch 1.5T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls SENSE Breast Coil 3.0T 7ch

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls SENSE Breast Coil

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls ST SENSE Breast Dx Coil

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls dS Breast 7ch 3.0T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls Mammotrak Diagnostic Coil 1.5T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls Mammotrak Interventional Coil 3.0T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls dS Breast 16ch 1.5T

November 4, 2024 · Medical device recalls Moderate risk Potential safety issue where a patient may be harmed while preparing for or dur…

Philips North America Llc recalls MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the in…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the i…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of t…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia Ambition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spect…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls SmartPath to dStream for 1.5T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images a…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia Elition X- For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls SmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain cross-sectional images, spectroscopic im…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or s…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spect…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…

Philips North America Llc recalls Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of…

September 3, 2024 · Medical device recalls Moderate risk Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and pro…