-
NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
IMPLANT EPIKUT PLUS MT16 3,5X10,0MM recall
FDA
· S.I.N. Implant System Ltda · Class II
-
Getinge 88-Series Washer- Disinfector recall
FDA
· Getinge Disinfection Ab · 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
-
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No recall
FDA
· Maquet Cardiovascular, LLC · 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
-
BeneVision N1 Patient Monitor (N1) recall
FDA
· Mindray North America · Class II
-
t:slim X2 Insulin Pump with Interoperable Technology (with Tandem t:slim… recall
FDA
· Tandem Diabetes Care, Inc. · Class II
-
Chromophare Surgical Light System recall
FDA
· Stryker Communications · Class II
-
Juggerknot Mini Soft Anchors, Model recall
FDA
· Biomet, Inc. · Class II
-
Extractor Pro RX Retrieval Balloon Catheter recall
FDA
· Boston Scientific Corporation · Class II
-
Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight recall
FDA
· Ortoma Ab · Class II
-
FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative, multiplexed… recall
FDA
· Biofire Defense · Class II
-
Voyant 1-Day Premium Toric, (stenfilcon A) contact lens recall
FDA
· CooperVision, Inc. · Class II
-
Sofmed Breathables, (stenfilcon A) contact lens recall
FDA
· CooperVision, Inc. · Class II
-
MyDay Toric, stenfilcon A) Contact Lens recall
FDA
· CooperVision, Inc. · Class II
-
STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device… recall
FDA
· Ethicon, LLC · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II