PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls
Every recall we track for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — 209 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them. 4 are rated “stop using now”.
Recalls per year, by danger level
Recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. more than tripled in 2025 (111, up from 23 in 2024). 2% rated “stop using now”.
All FDA recall records for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 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 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 3 | 1 | 0 | 4 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 10 | 14 | 0 | 24 |
| 2024 | 0 | 14 | 9 | 0 | 23 |
| 2025 | 4 | 81 | 25 | 1 | 111 |
| 2026 (to date) | 0 | 22 | 25 | 0 | 47 |
What to do if you have a recalled PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 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 MEDICAL SYSTEMS NEDERLAND B.V. recalls
59 shown- Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224,
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging equipment and solutions.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Jul 16, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software
PHILIPS
PHILIPSJul 16, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging systems and equipment. They provide a wide range of products including MRI, CT, X-ray, and ultrasound systems. Their products are used in hospitals and clinics worldwide for diagnostic imaging and patient care.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Jun 29, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion under the following System Descriptions and corresponding model numbers: 1. Azurion 3 M12; Model
Philips recalls Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, 7 B20, 7 M12, and 7 M20 X-ray systems with specific model numbers due to potential loss of imaging functionality from unauthorized hard drives.
PhilipsJun 17, 2026 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034
Philips recalls specific MultiDiagnost Eleva models due to hand switch button not fully releasing, which may cause loss of imaging or unintended radiation exposure. Affected models include 708032-708038.
PhilipsMay 18, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064,
Philips recalls Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, 7 B20, and 7 M12 models due to HDD performance degradation after 6 years of service, which may cause imaging or motorized movement failures. System restarts may temporarily restore function.
Philips Medical SystemsApr 30, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions
Philips recalls Azurion systems not configured with auxiliary pan handle due to mechanical wear in Float Tabletop control affecting table movements. Affected models include Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, B20, and 7 M12/M20 series with specific model numbers.
PhilipsApr 28, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12
Philips recalls Azurion 3 M12, 3 M15, 7 B12, 7 B20, 7 M12 and 7 M20 models (2016-2020) due to potential oil leakage in X-ray tube cooling units that may cause system to switch to low-dose fluoroscopy. No remedy provided.
PhilipsApr 28, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222,
Philips recalls Azurion 3 M12, M15, 5, 5 M12, 5 M20, 7, 7 B12, 7 B20, 7 M12, 7 M20 models due to potential loosening/breaking of cable hose carriers bolts and plastic parts when monitor is moved or rotated.
PhilipsMar 31, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to
Philips recalls AneurysmFlow software (model 001015) due to potential unreliable Mean Aneurysm Flow Amplitude (MAFA) ratio for aneurysm occlusion predictions. This could lead to incorrect clinical decisions during stent treatment.
PhilipsMar 19, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Vue Motion V12. Product Number: 1017979.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Mar 5, 2026 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
Philips recalls ALLURA Xper FD20 Biplane systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
PhilipsMar 3, 2026 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X,
Philips recalls Azurion 7 M12 systems with specific model numbers and software versions due to risk of unexpected table movement when pressing Reset Geometry button, even with lock engaged.
PhilipsJan 26, 2026 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10F; Model Number: 722002;
Philips recalls Allura Xper FD10F medical systems with model 722002 due to potential coolant contact with electrical components causing short circuits and system shutdowns.
PhilipsDec 15, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and
PHILIPS 722227 3D Ultrasound Scanner - High-resolution imaging for medical diagnostics
PHILIPSDec 12, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion system; Software Version Number: R3.1;
Philips recalls Azurion system software version R3.1 due to potential loss of X-ray imaging and motorized movement. Affected models include Azurion 3 M12, 3 M15, 5 M12, 5 M20, 7 M12, 7 M20, and 7 B12 systems with specific serial numbers.
PhilipsDec 12, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12.
Philips recalls Azurion Systems R3.0 models (722229-722234) due to 9 software issues that may cause image loss, system restarts, and misalignment. Affected units include Azurion 3 M12 through 7 M20 models with specific UDI numbers.
PhilipsDec 8, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Philips recalls Azurion 7M20 systems with FlexArm ceiling mounts due to inconsistent motor movement from grease leakage causing lubrication issues. Affected models include 722234.
PhilipsOct 2, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system
Philips recalls Zenition 50 interventional fluoroscopic x-ray systems with product number 718096 due to potential corrosion causing image quality problems. Affected units may need repair or replacement.
PhilipsSep 29, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842,
Philips recalls Allura Xper FD10 medical imaging systems with model numbers 722003, 722010, and 722026 due to potential BIOS battery depletion causing system shutdown without warning.
PhilipsSep 3, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers: K102005, K130842, K130638,
Philips recalls Allura Xper FD20 Biplane models with product codes 722013 and 722008 due to potential internal component failure affecting system performance. Imaging remains functional but motorized movements may become unavailable.
Philips Medical SystemsSep 3, 2025 - Lower riskMedical device
Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular, Software 8.0.0.4.
Philips recalls IntelliSpace Cardiovascular software version 8.0.0.4 due to outdated information display. Affected units may show incorrect data during medical procedures.
PhilipsAug 8, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the following with corresponding
Philips recalls specific models of interventional fluoroscopic X-ray systems due to potential missing air baffle component. Affected units include Allura Xper FD10, FD20, and Biplane models with listed serial numbers. Contact Philips for details.
PhilipsAug 1, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x, R2.x). Labeled as the following with
Philips recalls Azurion imaging systems (R1.x, R2.x) configured with 1-Phase UPS units that may shut down or fail to start during power loss. Affected models include Azurion 3 M12, 3 M15, 7 B12, 7 B20, 7 M12, 7 M20, and others with specific model numbers and serial ranges.
PhilipsAug 1, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 722026. 2. Allura Xper
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging systems and solutions. They provide advanced imaging equipment for hospitals and healthcare facilities worldwide.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Jun 30, 2025 - UnratedMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20. Fluoroscopic X-Ray System.
Philips recalls Azurion 7 M20 fluoroscopy systems with potential loose bolts connecting the C-arm gearbox to mounting flange. Affected units have specific serial numbers. No remedy stated in recall notice.
PhilipsJun 4, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion R1.x and R2.x systems; Model Numbers: (1) 722063, (2) 722064, (3) 722067, (4) 722068, (5) 722078, (6) 722079,
Philips recalls Azurion R1.x and R2.x medical imaging systems with specific model numbers due to software issues that may delay critical treatments, risking serious health outcomes like death in urgent medical scenarios.
PhilipsMay 28, 2025 - Lower riskMedical device
Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089.
Philips recalls specific software versions for IntelliSpace Cardiovascular systems due to potential missing or incomplete report data. Affected units may require updates to prevent inaccurate medical reports.
PhilipsApr 7, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Intera 1.5T Master/Nova, Model Number: 781106;
Philips recalls Intera 1.5T Master/Nova MRI scanners with model 781106 due to potential sharp edges from faulty coil seals that could cause skin abrasions or lacerations during scans.
PhilipsMar 24, 2025 - Use cautionMedical device
Philips Medical Systems Nederland B.V. recalls Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334;
Philips recalls Spectral CT on Rails with software version 5.1.0 (model 728334) due to unintended device movement during scans. Affected units may cause scanning errors or safety issues.
PhilipsFeb 28, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013.
Philips recalls Allura Xper FD20 Biplane models with specific catalog numbers due to potential patient falls from the table. Learn how to identify affected units and what to do.
PhilipsJan 13, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12 System Code: (1) 722063 (2) 722221
Philips recalls Azurion 3 M12 systems with specific serial numbers due to risk of finger entrapment between table rails during patient repositioning. Affected units may cause finger injury to operators and service personnel.
PhilipsJan 13, 2025 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Number: 722010. 2. Allura
Philips recalls Allura Xper Systems (R7.6-R8.1) with potential propeller motor clamping bolt and x-ray tube locking bolt failures causing erratic c-arm movements, collision risks, and image noise. Affected models include Allura Xper FD10, FD20, and FD20 Biplane with specific model numbers and serial ranges.
PhilipsNov 11, 2024 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Zenition 50, Model Number: 718096
Philips recalls Zenition 50 MRI scanners (model 718096) due to potential fuse blowing during start-up or procedures. Affected units have specific serial numbers listed in the recall notice.
PhilipsOct 7, 2024 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 M20 722236 Azurion 7 B20 722235 Azurion 7 B12 722234 Azurion 7
Philips recalls Azurion 7 M20, 5 M20, and 7 B20 models due to potential cable hose detachment from broken plastic or bolts, which could cause parts to fall and injure users.
PhilipsAug 22, 2024 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System, Model Numbers 722010,
Philips recalls Allura Xper systems (R8.1 with Poly-G Stand) due to incorrect bolt in LTE kits. Model numbers 722010, 722012, 722013; serial numbers 111 138 467 817 2928 269. Affected units may have safety risks during use.
PhilipsAug 8, 2024 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model
Philips recalls Azurion 7M20 systems with FlexArm ceiling-mounted systems due to potential inconsistent motorized movement from grease leakage causing lubrication issues.
PhilipsAug 6, 2024 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Interventional Fluoroscopic X-ray System with Software Version Number: R1.0, R1.1, R1.2- Intended for
Philips recalls Azurion Interventional Fluoroscopic X-ray Systems with software versions R1.0, R1.1, or R1.2 due to potential loss of X-ray imaging functionality and longer cold restart times.
PhilipsJul 15, 2024 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010, Software Version Number 8.1.100.
Philips recalls Allura Xper FD10 systems with ADN7NT patient tables (model 722010, software 8.1.100) due to risk of unintended table movement after software update. Affected units may require repair or replacement.
PhilipsMay 16, 2024 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of
Philips recalls certain versions of Interventional Hemodynamic Application software (R.1.2X, R.1.3.0, R1.2.1) due to potential pressure wave data synchronization errors between devices.
PhilipsMay 2, 2024 - Lower riskMedical device
Philips Medical Systems Nederland B.V. recalls Philips IntelliSpace Cardiovascular software, Model 830089.
Philips recalls software version 7.0.0.0 (UDI 0100884838115378) due to inability to archive, copy, or export study data. Affected users should contact Philips for details.
PhilipsApr 4, 2024 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive
Philips recalls Azurion 7 surgical imaging systems with Certeray generator due to risk of power loss from short circuits in the power inverter board, which could delay or terminate procedures.
PhilipsFeb 6, 2024 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules)
Philips recalls specific Allura Xper Interventional Fluoroscopic X-ray Systems with DIMMs that may stop functioning, causing procedure delays. Affected models include Allura Xper FD10, FD10/10, FD10C, FD20, and FD20/20 series with listed serial numbers.
PHILIPSJan 2, 2024 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the
Philips recalls Azurion Interventional Fluoroscopic X-ray Systems with specific disk bay models due to potential system failure during procedures. Affected units include Azurion 3 M12, M15, 5 M20, and 7 B12/B20/M12/M20 models with listed serial numbers.
PhilipsJan 2, 2024 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the
Philips recalls certain Azurion Interventional Fluoroscopic X-ray Systems where the framegrabber card may cause distorted or no images on the monitor, potentially delaying procedures.
PhilipsJan 2, 2024 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion system, Interventional fluoroscopic x-ray system. System Product Name - Model Numbers Azurion 3M12
Philips recalls Azurion 3M12, 3M15, 5M12, 5M20, 7B12/12, 7B20/15, 7M12, and 7M20 models due to potential imaging restarts during procedures, risking delays or aborted medical procedures.
PhilipsDec 12, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
Philips recalls Azurion 7 M20 FlexArm systems with specific software versions due to connectivity issues between the FlexArm and Maquet Magnus Table, potentially causing loss of movement.
PhilipsDec 8, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
Philips recalls Azurion 7 M20 FlexArm systems with specific Maquet Magnus Table software versions due to potential connectivity loss between components. Affected units have unique serial numbers and system codes.
PhilipsDec 8, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6
Philips recalls Azurion 3M15 models with specific software versions due to dark images appearing after pedal taps during fluoroscopy runs.
PhilipsDec 7, 2023 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion 7 M12 722079 Azurion 7 M20 722223 Azurion 7
Philips recalls Azurion 7 and 5 models with monoplane ceiling mounts that could fall if colliding with hospital equipment, risking injury or sterility issues.
PhilipsNov 3, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems
Philips recalls specific medical imaging systems due to a damaged foot switch that may cause no or intermittent x-ray radiation initiation. Affected models include Allura Xper, Allura Centron, and others. No remedy specified in official notice.
PhilipsAug 15, 2023 - Use cautionMedical device
Philips Medical Systems Nederland B.V. recalls Zenition 70. The device is to be used in health care facilities both inside and outside the operating room, sterile as
Philips recalls Zenition 7:0 medical imaging systems with Vascular Extension option and Wireless Foot Switch due to potential unintended radiation exposure in healthcare settings.
PhilipsJul 20, 2023 - Use cautionMedical device
Philips Medical Systems Nederland B.V. recalls Allura Xper series
Philips recalls Allura Xper series devices due to risk of unintended radiation emission when foot switch pedal gets stuck. Affected units may cause radiation exposure during use.
PhilipsJul 19, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems
Philips recalls wireless foot switches for Allura Xper and Azurion X-ray systems due to potential loss of availability during procedures. Affected models include 722001-722079.
PhilipsJun 30, 2023 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20. X-ray Image guided Therapy System.
Philips recalls Azurion 7 M20 X-ray systems with potential loose bolts and cracks in the FlexMove Carriage that could cause malfunction during use.
PhilipsJun 12, 2023 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion System with software versions: R2.2.O, R2.2.1, R2.2.3, R2.2.5 and R2.2.6. Models/Model Number: (1)
Philips recalls Azurion system models with specific software versions due to potential X-ray interruption when disk space is full. Affected units may experience sudden procedure halts during medical imaging.
PhilipsMar 21, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls SmartPerfusion, release R1.0, R1.1, R1.1.1, R1.1.5, R1.1.5.1 and R1.1.6
Philips recalls specific SmartPerfusion software versions due to potential inaccurate medical imaging results. Affected users should check their software version and contact Philips for updates.
PhilipsFeb 20, 2023 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Zenition 50, Model #718096
Philips recalls Zenition 50 surgical systems with wireless foot switch model #718096 due to firmware issues that may cause procedure delays if the hand or wired switches aren't used.
PhilipsDec 2, 2021 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion systems with software release R1.x
Philips recalls Azurion systems with software release R1.x due to a defect causing incorrect patient type selection during studies, potentially affecting dose control. Affected units may need correction.
PhilipsMay 26, 2021
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recall questions
How many recalls has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. had?
209 recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. are on record with U.S. safety agencies, from 2021–2026.
What is the most recent PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recall?
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224,, dated Jul 16, 2026. Every PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recall is listed on this page, newest first.
What should I do if I have a recalled PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 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 MEDICAL SYSTEMS NEDERLAND B.V. 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.