-
Allura Xper FD20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10F recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10C recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Zenition 50 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Cardio Vascular-Allura Centron recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper CV20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10C recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura CV20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
IntelliSpace Cardiovascular, Software 8.0.0.4 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Allura System configured with a 1 Phase UPS… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion System configured with a 1 Phase UPS… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Allura R8.2.x Systems recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 7 M20. Fluoroscopic X-Ray System recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion R1.x and R2.x systems recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
SmartPath to dStream for 3.0T, Model Number: 782145 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
SmartPath to dStream for 1.5T, Model Number: 782146 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera CV, Model Number: 781107 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 3.0T Quasar Dual, Model Number: 781150 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T R11, Model Number: 781170 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Power/Pulsar, Model Number: 781105 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Omni/Stellar, Model Number: 781104 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Master/Nova, Model Number: 781106 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Explorer/Nova Dual, Model Number: 781108 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II