19 Aug 2026 Device CLASS II Philips Azurion recalled by Philips Medical Systems Philips Medical Systems Nederl Potency & Assay 19 Aug 2026 Device CLASS II Allura Xper FD recalled by Philips Medical Systems Philips Medical Systems Nederl Other Nationwide 12 Aug 2026 Device CLASS II Philips Allura, Cardio Vascular-Allura Centron recalled Philips Medical Systems Nederl Other Nationwide 24 Jun 2026 Device CLASS II Philips Allura Xper with the following recalled Philips Medical Systems Nederl Other 24 Jun 2026 Device CLASS II Philips MultiDiagnost Eleva with the following recalled Philips Medical Systems Nederl Other 10 Jun 2026 Device CLASS II Philips Azurion 5M12 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 7B20/15 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 7M20 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 5M20 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 7M12 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 7B12/12 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 3M12 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 10 Jun 2026 Device CLASS II Philips Azurion 3M15 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 27 May 2026 Device CLASS II Integris-Allura system recalled by Philips Medical Systems Philips Medical Systems Nederl Packaging Defects Nationwide 27 May 2026 Device CLASS II Azurion system recalled by Philips Medical Systems Philips Medical Systems Nederl Packaging Defects Nationwide 20 May 2026 Device CLASS II Philips Azurion recalled by Philips Medical Systems Philips Medical Systems Nederl Foreign Material Nationwide 22 Apr 2026 Device CLASS II Philips AneurysmFlow recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper; System recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Azurion 7 B12 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper FD10C recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Vue Motion V12 recalled by Philips Medical Systems Philips Medical Systems Nederl Other Nationwide 8 Apr 2026 Device CLASS II Azurion 7 M20 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper; System recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper FD20/20 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper FD20/15 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper OR Table recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper/10 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Allura Xper FD20/20 OR Table recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Azurion 5 M20 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide 8 Apr 2026 Device CLASS II Azurion 7 M12 recalled by Philips Medical Systems Philips Medical Systems Nederl Device Malfunction Nationwide