| Philips Allura under the following System Descriptions and corresponding model numbers: 1. recall (Z-2891-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-08-05 |
| Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluor recall (Z-2893-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-08-05 |
| Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C recall (Z-2412-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-06-16 |
| Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), A recall (Z-2258-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-05-28 |
| Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, recall (Z-2259-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-05-28 |
| Product Name: Allura Xper FD10C; Model number: 722001; recall (Z-1062-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10F; Model Number: 722002; recall (Z-1063-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10; Model Number: 722003; recall (Z-1064-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10/10; Model Number: 722005; recall (Z-1065-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20; Model Number: 722006; recall (Z-1066-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20 Biplane; Model Number: 722008; recall (Z-1067-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10; Model Number: 722010; recall (Z-1068-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10/10; Model Number: 722011; recall (Z-1069-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20; Model Number: 722012; recall (Z-1070-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20 Biplane; Model Number: 722013; recall (Z-1071-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20 OR Table; Model Number: 722023; recall (Z-1072-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10; Model Number: 722026; recall (Z-1073-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10/10; Model Number: 722027; recall (Z-1074-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20; Model Number: 722028; recall (Z-1075-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20/10; Model Number: 722029; recall (Z-1076-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD20/20; Model Number: 722038; recall (Z-1077-2026) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2026-01-13 |
| Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbe recall (Z-2623-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005; Associated 510(k) nu recall (Z-2624-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033; Associated 510(k) numbers: recall (Z-2625-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbe recall (Z-2626-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers: recall (Z-2627-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015; Associated 510 recall (Z-2628-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025; Associated 510(k) recall (Z-2629-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20/20; Product Code: 722038; Associated 510(k) numbers: K102005, K130842, K1 recall (Z-2630-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20/20 OR Table; Product Code: 722039; Associated 510(k) numbers: K102005, K1 recall (Z-2631-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K1 recall (Z-2632-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20/15; Product Code: 722058; Associated 510(k) numbers: K102005, K130842, K1 recall (Z-2633-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura Xper FD20/15 OR Table; Product Code: 722059; Associated 510(k) numbers: K102005, K1 recall (Z-2634-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K recall (Z-2635-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-25 |
| Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the foll recall (Z-2504-2025) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2025-09-03 |
| Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay o recall (Z-1144-2024) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2024-02-16 |
| Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay o recall (Z-1151-2024) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2024-02-16 |
| Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dua recall (Z-1156-2024) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2024-02-16 |
| Allura Xper FD10 and FD20. X-ray Imaging System. recall (Z-2283-2023) | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. | 2023-08-02 |