-
MR 5300; Model Numbers: (1) 782110, (2) 782152 recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition X recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition S recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition X recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T CX recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T CX recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition S recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T S recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 3.0T recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 1.5T recall
FDA
· Philips North America Llc · Class II
-
Upgrade to MR 7700 recall
FDA
· Philips North America Llc · Class II
-
SmartPath to Ingenia Elition X recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for XR and 3.0T recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 3.0T recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 1.5T recall
FDA
· Philips North America Llc · Class II
-
Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) recall
FDA
· Cook Incorporated · Class II
-
Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) recall
FDA
· Cook Incorporated · Class II
-
True 3D Viewer, Model: EP-00003 recall
FDA
· Echopixel, Inc. · Class II
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter, Inc. · 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
-
Intera 1.5T, Model Numbers: 781195 and 781295 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.0T Power/Pulsar, Model Number: 781103 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.0T Omni/Stellar, Model Number: 781102 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 0.5T Standard, Model Number: 781101 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Enterprise 1.5T, Model Number: 781145 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
KliniTray Platte Faxitron ,groB "R" sterile recall
FDA
· Klinika Mdical Gmb · Class II
-
KliniTray recall
FDA
· Klinika Mdical Gmb · Class II
-
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395 recall
FDA
· Medline Industries, LP · Class II
-
Centurion Sterile Weitlaner Retractor, Reorder: 67315 recall
FDA
· Medline Industries, LP · Class II
-
CMS8000 Patient Monitor recall
FDA
· Contec Medical Systems Co., Ltd. · Class II
-
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety… recall
FDA
· ICU Medical, Inc. · Class II
-
Tornado Embolization Microcoil, intended for embolization of selective… recall
FDA
· Cook Incorporated · Class II
-
Augmedics Perc Pin Adaptor, Model recall
FDA
· Augmedics Ltd. · Class II
-
BIB Balloon in Balloon Dilatation Catheter recall
FDA
· Numed Inc · Class II
-
PiezoWave 2 Control Unit, Product Number 100506US… recall
FDA
· Richard Wolf GmbH · Class II
-
Pruitt Irrigation Occlusion Catheter recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Pruitt Occlusion Catheter recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
TufTex Over-the-Wire Embolectomy Catheter recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096… recall
FDA
· Abbott Molecular, Inc. · Class II
-
Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090… recall
FDA
· Abbott Molecular, Inc. · Class II
-
FoundationOne Companion Diagnostic (F1CDx) recall
FDA
· Foundation Medicine, Inc. · Class II
-
Contour Product Name: Contour Gold Eyelid Weight Model recall
FDA
· Meddev Corp · Class II
-
Contour Product Name: Contour Gold Eyelid Weight Model recall
FDA
· Meddev Corp · Class II
-
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit recall
FDA
· AVID Medical, Inc. · Class II
-
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit recall
FDA
· AVID Medical, Inc. · Class II
-
Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit recall
FDA
· AVID Medical, Inc. · Class II
-
IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Atalante X, Powered Exoskeleton recall
FDA
· Wandercraft Sas · Class II
-
Blueprint Software, BPUE001. Intended for use by surgeons as a pre… recall
FDA
· Tornier S.A.S. · Class II
-
Introducer Kit- Tearaway MicroSlide recall
FDA
· Galt Medical Corporation · Class II