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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Recalls
209 recalls on record · February 23, 2022 to August 19, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15 OR Table; System Code: 722059;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; System Code: 722058;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; System Code: 722039;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; System Code: 722038;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; System Code: 722029;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10F; System Code: 722002;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; System Code: 722001;
Hazard: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions:
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - Al
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
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, R2.
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number -
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X,
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
January 28, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion system; Software Version Number: R3.1;
Hazard: Philips has identified two (2) software issues affecting device systems that may result in loss of imaging (X-ray) functionality and/or loss of motorized movement, and/or incorrect image content and/or loss of data. Issue 1 - System remains in continuous restart mode after the start-up. Issue 2 - Longitudinal Position Error Applicable only to systems with Poly-G3 frontal stand.
January 21, 2026Medical DevicesFDA
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 corres
Hazard: Six (6) identified software issues which may result in the following: system keeps restarting, AMC triple drive, C-Partition of Suite PC running out of free space, system remains in continuous restart mode after the start-up, misalignment of Market Tool Overlay, and longitudinal positional error.
January 21, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. M
Hazard: Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on the FlexVision monitor, system continues to restart, AMD triple drive, C-Partition of Suite PC running out of free space, system remains in continuous restart mode after start-up, misalignment of Marker Tool Overlay, longitudinal position error.
January 21, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Model Number: 722038;
Hazard: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
January 21, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Model Number: 722029;
Hazard: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.