PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls

160 recalls on record · latest: April 30, 2026

Official U.S. recall history for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., compiled from official government records.

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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR…

April 30, 2026 · Medical device recalls Moderate risk It was identified that HDDs used in the PCs of Azurion and Allura systems may s…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222)…

April 30, 2026 · Medical device recalls Moderate risk It was identified that HDDs used in the PCs of Azurion and Allura systems may s…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura…

April 28, 2026 · Medical device recalls Moderate risk The deaeration hose in X-ray tube cooling units type CU3101, manufactured betwe…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Inte…

April 28, 2026 · Medical device recalls Moderate risk The deaeration hose in X-ray tube cooling units type CU3101, manufactured betwe…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions a…

April 28, 2026 · Medical device recalls Moderate risk Potential safety issue with Philips Azurion systems, where longitudinal and tra…

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…

April 28, 2026 · Medical device recalls Moderate risk The deaeration hose in X-ray tube cooling units type CU3101, manufactured betwe…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230)…

March 31, 2026 · Medical device recalls Moderate risk Potential for the bolts and plastic parts of the Cable Hose Carriers that hold…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to…

March 19, 2026 · Medical device recalls Moderate risk Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Vue Motion V12. Product Number: 1017979.

March 5, 2026 · Medical device recalls Moderate risk Potential that mis-ordered frames in Vue Motion during dynamic cine runs may ca…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; System Code: 722001;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; System Code: 722038;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; System Code: 722058;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; System Code: 722039;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; System Code: 722029;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10F; System Code: 722002;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M12; System Code: (1)722227, (2)722231;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15 OR Table; System Code: 722059;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;

March 3, 2026 · Medical device recalls Moderate risk Philips has identified instances where X-ray imaging may not be initiated or ma…

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:…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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.X…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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, R…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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 -…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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, R2…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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 - All…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

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.X…

January 26, 2026 · Medical device recalls Moderate risk Under certain conditions, the table may move unexpectedly when the Reset Geomet…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Model Number: 722006;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Number: 722026;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Model Number: 722013;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table; Model Number: 722023;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Model Number: 722008;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Number: 722010;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Model Number: 722029;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Model Number: 722012;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Model Number: 722005;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Model Number: 722038;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Model Number: 722011;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Number: 722003;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Product Name: Allura Xper FD10C; Model number: 722001;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Model Number: 722028;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Model Number: 722027;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10F; Model Number: 722002;

December 15, 2025 · Medical device recalls Moderate risk Philips has identified that in a limited number of impacted systems the drip tr…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion system; Software Version Number: R3.1;

December 12, 2025 · Medical device recalls Moderate risk Philips has identified two (2) software issues affecting device systems that ma…

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 corre…

December 12, 2025 · Medical device recalls Moderate risk Six (6) identified software issues which may result in the following: system ke…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Mod…

December 8, 2025 · Medical device recalls Moderate risk Nine (9) identified software issues which may result in the following: loss of…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;

October 2, 2025 · Medical device recalls Moderate risk The motorized longitudinal movement of the FlexArm stand may be inconsistent (n…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system

September 29, 2025 · Medical device recalls Moderate risk Over time some systems may experience loss of imaging functionality and/or poor…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Model Numbers: (1) 722005, (2) 722011, (3) 722027; Associated 510(k)s: K102005, K130638, K130842,…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842, K13…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table; Model Numbers: (1) 722015, (2) 722023, (3) 722035; Associated 510(k)s: K102005, K130638, K13…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15 OR Table; Model Numbers: 722059; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Cardio Vascular-Allura Centron; Model Numbers: 722400; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979,…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Model Numbers: 722038; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Model Numbers: (1) 722008, (2) 722013; Associated 510(k)s: K102005, K130638, K130842, K133292…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper CV20; Model Numbers: 722031; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K130842…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 OR Table; Model Numbers: 722033; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; Model Numbers: 722039; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Model Numbers: 722029; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; Model Numbers: 722058; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

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, K13…

September 3, 2025 · Medical device recalls Moderate risk The BIOS battery may deplete faster than initially anticipated during the desig…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Product Code: 722038; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbers: K102005, K130842, K130638…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025; Associated 510(k) numbers: K102005, K130842, K1…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; Product Code: 722039; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015; Associated 510(k) numbers: K102005, K130842…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842, K130638…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K16…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033; Associated 510(k) numbers: K102005, K130842, K130638, K…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15 OR Table; Product Code: 722059; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005; Associated 510(k) numbers: K102005, K130842, K130…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; Product Code: 722058; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers: K102005, K130842, K130638, K1…

September 3, 2025 · Medical device recalls Moderate risk Systems may not perform as intended due to the deterioration of certain interna…

Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular, Software 8.0.0.4.

August 8, 2025 · Medical device recalls Moderate risk Software issue that results in the display of outdated information.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the following with corresponding mode…

August 1, 2025 · Medical device recalls Moderate risk Potential that a component (air baffle) may be missing in some Nehalem FlexVisi…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x, R2.x). Labeled as the following with correspo…

August 1, 2025 · Medical device recalls Moderate risk Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Po…

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 corres…

August 1, 2025 · Medical device recalls Moderate risk Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Po…

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 FD10/…

June 30, 2025 · Medical device recalls Moderate risk Potential for temporary loss of imaging (X-ray) functionality due to software i…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20. Fluoroscopic X-Ray System.

June 4, 2025 · Medical device recalls Moderate risk Potential for bolts connecting the gearbox to the mounting flange of the C-arm…

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, (…

May 28, 2025 · Medical device recalls Moderate risk A software issue was identified in the internal communication process between t…

Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089.

April 7, 2025 · Medical device recalls Moderate risk An issue was identified with the software when using the Echo Module of ISCV, t…

Intera CV recalled over laceration hazard

March 24, 2025 · Medical device recalls Moderate risk The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges tha…

Intera 1 recalled over laceration hazard

March 24, 2025 · Medical device recalls Moderate risk The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges tha…

Intera 1 recalled over laceration hazard

March 24, 2025 · Medical device recalls Moderate risk The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges tha…

Intera 1 recalled over laceration hazard

March 24, 2025 · Medical device recalls Moderate risk The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges tha…