| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 an | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 an | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-03 | FDA Device | FDA Recall: Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), A | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-06-03 | FDA Device | FDA Recall: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-05-27 | FDA Device | FDA Recall: Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-N | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-05-27 | FDA Device | FDA Recall: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (7220 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-05-27 | FDA Device | FDA Recall: Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below pro | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-05-27 | FDA Device | FDA Recall: Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | Class II | N/A |
| 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: 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 FD10 OR Table; System Code: (1) 722022, (2)722033; | 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 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: 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 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: 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 |