Brand

Philips North America Recalls

82 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Philips North America.

82Total Recalls
20Critical
269,405Units Affected
Apr 14, 2026Most Recent
All Recalls

Every Philips North America Recall

Sorted by most recent. Click any recall for full details.

82 recalls
High RiskFDA
Philips North America
Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
Medical Devices·119 affected·Jan 3, 2024
High RiskFDA
Philips North America
Achieva XR. Model (REF) Numbers 781153, 781253.
Medical Devices·23 affected·Jan 3, 2024
High RiskFDA
Philips North America
Achieva 1.5T Initial system. Model (REF) Numbers 781178.
Medical Devices·23 affected·Jan 3, 2024
RecallFDA
Philips North America
Achieva 3.0T, Model No. 781177
Medical Devices·7 affected·Dec 29, 2023
RecallFDA
Philips North America
SmartPath to dStream for 1.5T, Model No. 781260, 782112
Medical Devices·7 affected·Dec 29, 2023
RecallFDA
Philips North America
Intera 1.5T, Model No. 781195
Medical Devices·7 affected·Dec 29, 2023
CriticalFDA
Philips North America
BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 4535...
Medical Devices·302 affected·Dec 15, 2023
High RiskFDA
Philips North America
ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
Diagnostic Devices·20 affected·Dec 15, 2023
High RiskFDA
Philips North America
ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
Diagnostic Devices·151 affected·Dec 15, 2023
CriticalFDA
Philips North America
BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 453560749161
Medical Devices·106 affected·Dec 15, 2023
CriticalFDA
Philips North America
BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;
Medical Devices·56 affected·Dec 15, 2023
High RiskFDA
Philips North America
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
Medical Devices·55 affected·Dec 7, 2023
High RiskFDA
Philips North America
BrightView X, Gamma Camera, Product Code 882478
Medical Devices·59 affected·Nov 30, 2023
High RiskFDA
Philips North America
BrightView, Gamma Camera System, Product Code 882480.
Medical Devices·359 affected·Nov 30, 2023
High RiskFDA
Philips North America
BrightView XCT, Gamma Camera, Product Code 882482
Medical Devices·135 affected·Nov 30, 2023
High RiskFDA
Philips North America
(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Mod...
Medical Devices·41 affected·Nov 28, 2023
High RiskFDA
Philips North America
Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Medical Devices·1 affected·Oct 9, 2023
High RiskFDA
Philips North America
Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Medical Devices·1 affected·Oct 9, 2023
High RiskFDA
Philips North America
Allura Xper IGTS Fixed Systems
Medical Devices·0 affected·Oct 4, 2023
High RiskFDA
Philips North America
BV Endura, BV Pulsera Philips Image Guided Therapy-Systems (IGTS)Mobile Surgery C-arm systems.
Medical Devices·0 affected·Oct 4, 2023
High RiskFDA
Philips North America
Veradius Unity Mobile Surgery C-arm
Medical Devices·0 affected·Oct 4, 2023
High RiskFDA
Philips North America
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
Medical Devices·601 affected·Jun 12, 2023
High RiskFDA
Philips North America
MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Medical Devices·601 affected·Jun 12, 2023
High RiskFDA
Philips North America
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
Medical Devices·640 affected·Jun 12, 2023
High RiskFDA
Philips North America
MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Medical Devices·640 affected·Jun 12, 2023
High RiskFDA
Philips North America
Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146
Medical Devices·20 affected·Apr 25, 2023
High RiskFDA
Philips North America
Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
Medical Devices·591 affected·Apr 19, 2023
High RiskFDA
Philips North America
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
Medical Devices·3 affected·Mar 20, 2023
High RiskFDA
Philips North America
ProxiDiagnost N90 R.1.0
Diagnostic Devices·25 affected·Mar 3, 2023
High RiskFDA
Philips North America
CombiDiagnost R90 R.1.0
Diagnostic Devices·25 affected·Mar 3, 2023
High RiskFDA
Philips North America
CombiDiagnost R90 R1.1
Diagnostic Devices·25 affected·Mar 3, 2023
High RiskFDA
Philips North America
Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Medical Devices·10 affected·Jan 6, 2022
High RiskFDA
Philips North America
Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Medical Devices·1 affected·Jan 6, 2022
High RiskFDA
Philips North America
(1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)
Medical Devices·56 affected·Jul 15, 2021