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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall VNS Therapy AspireHC Pulse Generator Neurological Devices Cyberonics, Inc 3 United States USFDA
Device Recall Trilogy Bone Screws Orthopedic Devices Zimmer Manufacturing B.V. 2 United States USFDA
Device Recall Conformis iTotal CR G2 Knee Replacement System Orthopedic Devices ConforMIS, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall Osteobond Copolymer Bone Cement Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Persona Cemented Tibial Broach Inserter/Extractor Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall WECK Hemoclip General and Plastic Surgery Devices Teleflex Medical 2 United States USFDA
Device Recall Lotus Valve System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Lotus Valve System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Lotus Valve System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Sirius Polish Cemented Stem 34B Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Sirius Polish Cemented Stem 34B Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Arrow Gastroenterology-Urology Devices Arrow International Inc 2 United States USFDA
Device Recall Protg Rx Tapered Carotid Stent System Cardiovascular Devices Ev3, Inc. 3 United States USFDA
Device Recall Protg Rx Tapered Carotid Stent System Cardiovascular Devices Ev3, Inc. 3 United States USFDA
Device Recall SolitaireC Cervical Spacer System Orthopedic Devices Ebi, Llc 2 United States USFDA
Device Recall BIOLOX delta TS Ceramic Femoral Head Articul/eze 12/14 36mm 12 Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall TiBond Orthopedic Devices Spinal Elements, Inc 2 United States USFDA
Device Recall Timberline Anchored Lateral Retractable Drill Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Anchored Lateral Variable Retractable Sleeve Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Merlinhome RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0 Cardiovascular Devices St Jude Medical Cardiac Rhythm Management Division 3 United States USFDA