-
MiniMed 620G Insulin Pump (MMT-1750) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860… recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890… recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894… recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780… recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Vue Motion V12. Product Number: 1017979 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Jiffy Original Composite Polisher Cups (Coarse) 12pk recall
FDA
· Ultradent Products, Inc. · Class II
-
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit recall
FDA
· CareFusion 303, Inc. · Class II
-
Flexible Cryoprobe (OD 2.4mm, L1.15mm) recall
FDA
· Erbe USA Inc · Class I
-
Flexible Cryoprobe (OD 1.7mm, L1.15mm) recall
FDA
· Erbe USA Inc · Class I
-
Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) recall
FDA
· Erbe USA Inc · Class I
-
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing… recall
FDA
· Radnostix · Class III
-
Aptima HPV Assay Product Name: Aptima HPV Assay Model recall
FDA
· Hologic, Inc · Class II
-
Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion… recall
FDA
· Elekta, Inc. · Class II
-
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recall
FDA
· Winder Laboratories, LLC · Class III
-
Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes… recall
FDA
· Cardinal Health 200, LLC · Class I
-
CHEMISTRY ANALYZER AU5800 recall
FDA
· Beckman Coulter Mishima K.K. · Class II
-
DxC 700 AU recall
FDA
· Beckman Coulter Mishima K.K. · Class II
-
Owner's Booklets and Instructions for Use that are used with the following… recall
FDA
· Trividia Health, Inc. · Class I
-
Owner's Booklets and Instructions for Use that are used with the following… recall
FDA
· Trividia Health, Inc. · Class I
-
Owner's Booklets and Instructions for Use that are used with the following… recall
FDA
· Trividia Health, Inc. · Class I
-
Owner's Booklets and Instructions for Use that are used with the following… recall
FDA
· Trividia Health, Inc. · Class I
-
Equinoxe Product Name: Equinoxe Core Instrument Kit Model recall
FDA
· Exactech, Inc. · Class II
-
Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model recall
FDA
· Exactech, Inc. · Class II
-
Rosabella brand MORINGA recall
FDA
· Ambrosia Brands LLC · Class I
-
Sodium Iodide (I-131) Solution, Therapeutic Oral… recall
FDA
· Radnostix · Class II
-
Gerber Arrowroot Biscuits, Net Wt recall
FDA
· Nestle Infant Nutrition · Class II
-
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue… recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
FDA
· Elekta, Inc. · Class II
-
Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
FDA
· Elekta, Inc. · Class II
-
Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical 25GA Backflush, VS0270.25 recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical TID Pharos Illuminated Depressor, VS0801B recall
FDA
· Vortex Surgical Inc. · Class II
-
Rumex Disposable Diamond Dusted ILM Elevator, 12-7523 recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical I2 Injection Kit, VS0500 recall
FDA
· Vortex Surgical Inc. · Class II
-
Tecfen Retractable Membrane Polisher, QTPR1267-23 recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25 recall
FDA
· Vortex Surgical Inc. · Class II
-
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2… recall
FDA
· Vortex Surgical Inc. · Class II
-
25GA Subretinal Injection Cannula VS0220.25 recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive… recall
FDA
· Vortex Surgical Inc. · Class II
-
Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2… recall
FDA
· Vortex Surgical Inc. · Class II
-
Vortex Surgical 1. 23GA Laser Probe Curved Cat No recall
FDA
· Vortex Surgical Inc. · Class II
-
Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens recall
FDA
· Vortex Surgical Inc. · Class II
-
EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H recall
FDA
· Encore Medical, LP · Class II
-
EMPOWR 3D Knee Tibial Insert 5R 14MM, VE recall
FDA
· Encore Medical, LP · Class II
-
COULTER DxH Diluent recall
FDA
· Beckman Coulter, Inc. · Class II
-
*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm recall
FDA
· Boston Scientific Corporation · Class I
-
*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm recall
FDA
· Boston Scientific Corporation · Class I
-
HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm recall
FDA
· Boston Scientific Corporation · Class I
-
AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm recall
FDA
· Boston Scientific Corporation · Class I
-
AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm recall
FDA
· Boston Scientific Corporation · Class I
-
AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm recall
FDA
· Boston Scientific Corporation · Class I
-
Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg… recall
FDA
· Unichem Pharmaceuticals USA Inc. · Class II
-
AlternatiV+ Screw-In Anchor recall
FDA
· Aju Pharm Co., Ltd. · Class II
-
AlternatiV+ Max Knotless Anchor recall
FDA
· Aju Pharm Co., Ltd. · Class II
-
Genesis Push-In Suture Anchor recall
FDA
· Aju Pharm Co., Ltd. · Class II