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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall S2 Fluid Pack as a part of the cobas b221 Roche OMNI S systems Clinical Chemistry and Clinical Toxicology Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Device Recall Olympus Gastroenterology-Urology Devices Integrated Medical Systems Inc 2 United States USFDA
Device Recall Aurora, Caliente Aurora, PSX400, Mobile Beat Max, Mobile Beat Max MKII, Xbeam, and Hawk 500 models X-Laser Llc Not Classified United States USFDA
Sams Modular Perfusion System 8000 Cardiovascular Devices Terumo Cardiovascular Systems Corporation 2 United States USFDA
Dr Mullins Kit General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
BD AutoShield Pen Needle General Hospital and Personal Use Devices Becton Dickinson & Company 2 United States USFDA
King Systems Universal Flex2 Breathing Circuit Anesthesiology Devices King Systems Corp. 1 United States USFDA
Device Recall VenaCure EVLT General and Plastic Surgery Devices Angiodynamics Worldwide Headquarters 2 United States USFDA
Device Recall Symbiq Two Channel Infuser General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall da Vinci 5 mm Flared Instrument Cannulae General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Customed Ear, Nose, and Throat Devices Customed, Inc 1 United States USFDA
Device Recall IMHS CP Orthopedic Devices Smith & Nephew Inc 1 United States USFDA
Device Recall Hospira Primary I.V. set General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Synthes Implant Holder for Synfix (TM)LR Orthopedic Devices Synthes USA HQ, Inc. 1 United States USFDA
Hospitak Anesthesiology Devices Unomedical 2 United States USFDA