Philips North America, LLC
273 recalls on record · Latest: Dec 10, 2025
FDA Devices Moderate Dec 10, 2025
IntelliVue MP90. Product Number: M8010A.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP30. Product Number: M8002A.
FDA Devices Moderate Dec 10, 2025
IntelliVue Patient Monitor MX800. Product Number: 865240.
FDA Devices Moderate Dec 10, 2025
IntelliVue Patient Monitor MX700. Product Number: 865241.
FDA Devices Moderate Dec 10, 2025
CT 5300; Software Version Number: 4.5, 5.0, 5.1;
FDA Devices Moderate Dec 10, 2025
IntelliVue Patient Monitor MX500. Product Number: 866064.
FDA Devices Moderate Dec 10, 2025
IntelliVue Patient Monitor MX850. Product Number: 866470.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP2. Product Number: M8102A.
FDA Devices Moderate Dec 10, 2025
Incisive CT; Software Version Number: 4.5, 5.0, 5.1;
FDA Devices Moderate Dec 10, 2025
IntelliVue MP50. Product Number: M8004A.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP80. Product Number: M8008A.
FDA Devices Moderate Dec 10, 2025
IntelliVue Patient Monitor MX100. Product Number: 867033.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP40. Product Number: M8003A.
FDA Devices Moderate Dec 10, 2025
IntelliVue Multi Measurement Server X2. Product Number: M3002A.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP60. Product Number: M8005A.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP5. Product Number: M8105A.
FDA Devices Moderate Dec 10, 2025
IntelliVue MP20. Product Number: M8001A.
FDA Devices Moderate Dec 10, 2025
IntelliVue Patient Monitor MX600. Product Number: 865242.
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243. …
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number: 728246. …
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number: 728…
FDA Devices Moderate Oct 1, 2025
Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3…
FDA Devices Moderate Jul 2, 2025
Spectral CT. Computed tomography X-ray system.
FDA Devices Moderate May 28, 2025
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia 3.0T CX; Model Number: 781271;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia 1.5T CX; Model Number: 781262;
FDA Devices Moderate May 28, 2025
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia 1.5T S; Model Number: 781347;
FDA Devices Moderate May 28, 2025
Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
FDA Devices Moderate May 28, 2025
Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;
FDA Devices Moderate May 28, 2025
Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;
FDA Devices Moderate May 28, 2025
Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;
FDA Devices Moderate May 28, 2025
Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
FDA Devices Moderate May 14, 2025
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Ped…
FDA Devices Moderate Apr 30, 2025
Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical pr…
FDA Devices Moderate Apr 30, 2025
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical…
FDA Devices Moderate Apr 30, 2025
Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical p…
FDA Devices Moderate Apr 30, 2025
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
FDA Devices Moderate Apr 23, 2025
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
FDA Devices Moderate Feb 12, 2025
IntelliVue Patient Monitor MX400. Model Number: 866060
FDA Devices Moderate Feb 12, 2025
IntelliVue Patient Monitor MX450. Model Number: 866062
FDA Devices Moderate Feb 12, 2025
IntelliVue Patient Monitor MX550. Model Number: 866066
FDA Devices Moderate Feb 12, 2025