Philips North America recalls
Philips North America appears in 532 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Intera 1.5T Master/Nova, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Ingenia Ambition S, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Ingenia Elition S, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Intera 3.0T Quasar Dual, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Enterprise 1.5T, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Intera 1.5T Achieva IT Nova, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Ingenia Ambition X, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Intera 0.5T Standard, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Achieva 1.5T, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Ingenia 3.0T CX, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Ingenia 1.5T S, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System
FDA Device · Class II · 2024-04-24 · Philips North America - PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-…
FDA Device · Class II · 2024-04-17 · Philips North America - CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
FDA Device · Class II · 2024-04-03 · Philips North America - Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version…
FDA Device · Class II · 2024-04-03 · Philips North America - ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
FDA Device · Class II · 2024-02-21 · Philips North America - ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
FDA Device · Class II · 2024-02-21 · Philips North America - Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
FDA Device · Class II · 2024-02-14 · Philips North America - BrightView, gamma camera system
FDA Device · Class I · 2024-02-14 · Philips North America - BrightView XCT, gamma camera for SPECT
FDA Device · Class I · 2024-02-14 · Philips North America - Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
FDA Device · Class II · 2024-02-14 · Philips North America - Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
FDA Device · Class II · 2024-02-14 · Philips North America - BrightView X, gamma camera for SPECT
FDA Device · Class I · 2024-02-14 · Philips North America - Intera Achieva 1.5T Pulsar
FDA Device · Class II · 2024-02-07 · Philips North America - Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296
FDA Device · Class II · 2024-02-07 · Philips North America - Intera 1.5T Achieva Nova-Dual
FDA Device · Class II · 2024-02-07 · Philips North America - Intera 1.5T Achieva Nova
FDA Device · Class II · 2024-02-07 · Philips North America - Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105
FDA Device · Class II · 2024-02-07 · Philips North America - Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345
FDA Device · Class II · 2024-02-07 · Philips North America - SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129
FDA Device · Class II · 2024-02-07 · Philips North America - SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112
FDA Device · Class II · 2024-02-07 · Philips North America - Achieva XR. Model (REF) Numbers 781153, 781253
FDA Device · Class II · 2024-02-07 · Philips North America - Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261
FDA Device · Class II · 2024-02-07 · Philips North America - Achieva 1.5T Conversion
FDA Device · Class II · 2024-02-07 · Philips North America - Achieva 1.5T Initial system
FDA Device · Class II · 2024-02-07 · Philips North America - Intera 1.5T, Model No. 781195
FDA Device · Class III · 2024-01-31 · Philips North America - Ingenia Ambition X, Model No. 782109
FDA Device · Class III · 2024-01-31 · Philips North America - SmartPath to dStream for 1.5T, Model No. 781260, 782112
FDA Device · Class III · 2024-01-31 · Philips North America - Achieva 1.5T Conversion, Model No. 781283
FDA Device · Class III · 2024-01-31 · Philips North America - Achieva 1.5T, Model No. 781178, 781196, 781296
FDA Device · Class III · 2024-01-31 · Philips North America - Achieva 3.0T, Model No. 781177
FDA Device · Class III · 2024-01-31 · Philips North America - Incisive CT, Model Numbers 728144 and 728143
FDA Device · Class II · 2024-01-24 · Philips North America - (1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436
FDA Device · Class II · 2024-01-24 · Philips North America - Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System
FDA Device · Class II · 2024-01-24 · Philips North America - (1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model N…
FDA Device · Class II · 2024-01-24 · Philips North America - BrightView XCT, Gamma Camera, Product Code 882482
FDA Device · Class II · 2024-01-17 · Philips North America - BrightView, Gamma Camera System, Product Code 882480
FDA Device · Class II · 2024-01-17 · Philips North America - BrightView X, Gamma Camera, Product Code 882478
FDA Device · Class II · 2024-01-17 · Philips North America - (1) Ingenia Ambition X (Product Number 781356)
FDA Device · Class II · 2024-01-17 · Philips North America - The device is a whole-body CT x-ray system
FDA Device · Class II · 2023-12-27 · Philips North America