Philips North America recalls
Every recall we track for Philips North America — 140 in all, from 2020–2026 — plus the complaints and injury reports the public filed about them. 21 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Philips North America more than tripled in 2025 (45, up from 15 in 2024). 15% rated “stop using now”.
All FDA recall records for Philips North America since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 3 | 0 | 0 | 3 |
| 2023 | 1 | 24 | 12 | 5 | 42 |
| 2024 | 0 | 12 | 3 | 0 | 15 |
| 2025 | 20 | 8 | 16 | 1 | 45 |
| 2026 (to date) | 0 | 1 | 21 | 11 | 33 |
What to do if you have a recalled Philips North America product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Philips North America recalls
31 shown- Lower riskMedical device
Philips North America recalls Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T
Philips recalls Ingenia 3.0T and 3.0T CX MRI scanners with model numbers 781342, 781377, 782103, and 781271 due to incorrect diffusion tensor imaging data exports that may cause inaccurate nerve pathway mapping in brain imaging software.
PhilipsAug 28, 2026 - Lower riskMedical device
Philips North America recalls Philips Patient Information Center iX REF:866389
Philips recalls Patient Information Center iX software versions 4.0-4.: software may freeze and become unresponsive. Affected units: REF:866389 with UDI (01)00884838127067.
PhilipsJul 31, 2026 - Lower riskMedical device
Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.
Philips recalls SmartPath to dStream 3.0T with MR Elastography (MRE) model 782145 due to potential stiffness value errors from image reconstruction settings. Affected units may display incorrect voxel sizes in scans.
PhilipsApr 14, 2026 - Lower riskMedical device
Philips North America recalls Patient Information Center iX; Software Version Number: 4.5.0
Philips recalls Patient Information Center iX software version 4.5.0 due to upgrade notifications not informing users of changes. Affected units may require software updates to prevent unexpected system behavior.
PhilipsDec 22, 2025 - Lower riskMedical device
Philips North America recalls SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1.
Philips recalls SmartPath to dStream 3.0T MRI systems with software versions R11.1 and R12.1 due to potential stiffness value errors in MR Elastography images. Affected units may show inaccurate stiffness maps when viewed in PACS.
PhilipsDec 3, 2025 - Use cautionMedical device
Philips North America recalls Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM
Philips recalls Azurion R3.0 interventional fluoroscopy systems (model 722234) shipped between July 2024 and June 2025 due to missing SSD spacer, which could fail FDA safety requirements for source-skin distance.
PhilipsOct 27, 2025 - Lower riskMedical device
Philips North America recalls Cardiac Workstation 5000; Model Number: 860439;
Philips recalls Cardiac Workstation 5000 model 860439 due to power module wire failure causing short circuits. Affected units may have short circuits that could lead to equipment malfunction.
PhilipsSep 12, 2025 - Stop using nowMedical device
Philips North America recalls Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY);
Philips recalls Ingenia Elition X MRI scanners with specific model numbers (China only) due to potential fire from gradient coil failures. Affected units may produce smoke or fire.
PhilipsJun 30, 2025 - Stop using nowMedical device
Philips North America recalls Intera 1.5T Achieva Nova-Dual Product Number: 781173;
Philips recalls Intera 1.5T Achieva Nova-Dual MRI systems with specific serial numbers due to potential fire risk from gradient coil component failure. Affected units may produce smoke or fire, risking injury or death.
PhilipsMay 29, 2025 - Lower riskMedical device
Philips North America recalls IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500
Philips recalls IntelliVue Patient Monitors MX400, MX430, MX450, MX500, and MX550 models with potential grounding issues that could impact electromagnetic safety. Affected units were shipped after April 26, 2024.
PhilipsAug 30, 2024 - Lower riskMedical device
Philips North America recalls CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Philips recalls CareEvent Event Management System software version C.03.X for iOS devices with locked screens and passcodes. Custom ringtones won't play when iOS screens are locked with a passcode.
PhilipsFeb 28, 2024 - Use cautionMedical device
Philips North America recalls Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
Philips recalls Intera 1.5T Achieva Nova MRI scanners with model 781172 due to potential sharp edges from failing coil seal adhesive, which could cause skin injuries during scans.
PhilipsJan 3, 2024 - Use cautionMedical device
Philips North America recalls Achieva 3.0T, Model No. 781177
Philips recalls Achieva 3.0T MRI systems with Model No. 781177 due to a potentially dangerous electrical shock warning label error that could risk service personnel safety.
PhilipsDec 29, 2023 - Lower riskMedical device
Philips North America recalls ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
Philips recalls ProxiDiagnost upgrade A Multi-functional Radiography and Fluoroscopy systems due to potential incorrect patient data display and security vulnerabilities in wireless detectors.
PhilipsDec 15, 2023 - Use cautionMedical device
Philips North America recalls BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791
Philips recalls BrightView gamma camera systems with specific model numbers due to risk of detector falling, potentially causing injury to patient's lower limbs.
PhilipsDec 15, 2023 - Use cautionMedical device
Philips North America recalls Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
Philips recalls Incisive CT models 728143/728144 with specific PIM cable part numbers due to risk of ECG signal loss during emergencies. Affected units may require replacement of the cable to prevent delays in diagnosis.
PhilipsDec 7, 2023 - Use cautionMedical device
Philips North America recalls BrightView X, Gamma Camera, Product Code 882478
Philips recalls BrightView X Gamma Cameras with specific serial numbers due to potential patient injury risks during quality scans. The gap between patient support and detector may cause entrapment, fractures, or lacerations.
PhilipsNov 30, 2023 - Lower riskMedical device
Philips North America recalls (1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC
Philips recalls Patient Information Center iX models due to potential failure of push notifications, which could delay critical patient condition detection. Affected units include specific hardware and software versions sold in the U.S.
PhilipsNov 28, 2023 - Lower riskMedical device
Philips North America recalls Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Philips recalls Spectral CT on Rails with software version 5.1.0 (model 728334) due to potential software crashes during CCT Fluoroscopy mode activation. Affected units may require restart after crash.
PhilipsOct 9, 2023 - Use cautionMedical device
Philips North America recalls Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Philips recalls Spectral CT on Rails with software version 5.1.0 (model 728334) due to risk of gantry misalignment during scans, potentially causing incorrect scans or collisions. Affected units sold from 2020-2021.
PhilipsOct 9, 2023 - UnratedMedical device
Philips North America recalls Allura Xper IGTS Fixed Systems
Philips recalls Allura Xper IGTS Fixed Systems sold in Puerto Rico due to missing Source-to-Skin Distance Spacer (Tube-spacer). Affected models lack warning labels and require immediate attention.
PhilipsOct 4, 2023 - Use cautionMedical device
Philips North America recalls Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia
Philips recalls Ingenia Elition X MRI systems with specific product numbers due to risk of bypassing smoke detector interlock after power cycling.
PhilipsJun 12, 2023 - Lower riskMedical device
Philips North America recalls Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia
Philips recalls Ingenia Elition X MRI systems with specific product numbers due to potential improper installation of the SmokeDetector Interlock cable, which does not affect system functionality but may require service diagnostics.
PhilipsJun 12, 2023 - Use cautionMedical device
Philips North America recalls Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146
Philips recalls Incisive CT X-Ray System Model 728146 due to risk of metal mounting box detaching and causing injury or system shutdown. Affected units have specific serial numbers.
PhilipsApr 25, 2023 - Lower riskMedical device
Philips North America recalls Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390,
Philips recalls Patient Information Center iX (Product Code 866386) and iX Expand (866390) software version 4.0.1 due to DHCP lease expiration causing sync failures when reconnecting. Affected devices may need software update.
PhilipsApr 19, 2023 - Use cautionMedical device
Philips North America recalls Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
Philips recalls CT X-Ray System Model 72813 due to foot entrapment risk when pressing the unload pedal. Affected units have specific US and OUS serial numbers.
PhilipsMar 20, 2023 - Lower riskMedical device
Philips North America recalls ProxiDiagnost N90 R.1.0
Philips recalls ProxiDiagnost N90 R.1.0 devices missing FDA certification labels. Affected units may not meet regulatory standards. Consumers should check serial numbers listed in the recall notice.
PhilipsMar 3, 2023 - Use cautionMedical device
Philips North America recalls IntelliVue G7m Anesthesia Gas Module, Product Number 866173
Philips recalls IntelliVue G7m Anesthesia Gas Module (Product 866173) due to potential gas measurement interruption from a sample pump issue. Affected units may trigger inoperable alarms.
PhilipsJan 18, 2023 - Use cautionMedical device
Philips North America recalls Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation
Philips recalls Ingenia Ambition X patient transport systems with HA FlexTrak II accessory due to potential MRI safety risks from magnetic wheels. Affected units may be attracted to MRI machines if in the magnetic field.
PhilipsJan 6, 2022 - Use cautionMedical device
Philips North America recalls (1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)
Philips recalls Ingenia Ambition X and S MRI scanners with serial numbers 47000-47200 and 48000-48200 due to risk of uncontrolled shutdown if power fails, potentially causing safety issues.
PhilipsJul 15, 2021 - Use cautionMedical device
Philips North America recalls PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to
Philips recalls specific Incisive CT software versions due to risk of patient table moving during scans, potentially causing collisions with operators.
PhilipsDec 24, 2020
Philips North America recall questions
How many recalls has Philips North America had?
140 recalls from Philips North America are on record with U.S. safety agencies, from 2020–2026.
What is the most recent Philips North America recall?
Philips North America recalls Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T, dated Aug 28, 2026. Every Philips North America recall is listed on this page, newest first.
What should I do if I have a recalled Philips North America product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Philips North America recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.