PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Frequent Recalls

Recalls

Units Recalled

Injuries

Deaths

1 category · 2026-04-08 to 2026-04-22

Date	Source	Product	Brand	Severity	Units
2026-04-22	FDA Device	FDA Recall: Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Intervent	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Allura Xper FD20/10; System Code: 722029;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD10F; System Code: 722002;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Allura Xper FD20/15 OR Table; System Code: 722059;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 5 M12; System Code: (1)722227, (2)722231;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Allura Xper FD20/20 OR Table; System Code: 722039;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Allura Xper FD20/15; System Code: 722058;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Vue Motion V12. Product Number: 1017979.	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Allura Xper FD10C; System Code: 722001;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Allura Xper FD20/20; System Code: 722038;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Class II	N/A