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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Segmental fluted stem, 19x190mm str, Sterile, Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall Por fullct fem st 17x200mm, Sterile, Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall Platinium CRT DF1 1711 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall VERSYS BEADED FULLCOAT BOWED REVISION HIP PROSTHESIS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall Sigma Pacemaker Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Managment 3 United States USFDA
FLEXSTENT Femoropopliteal SelfExpanding Stent System (Clinical Study Protocol FSS0003 (OPEN trial) Cardiovascular Devices Cordis Corporation 3 United States USFDA
BIOMET Comprehensive Shoulder System Orthopedic Devices Biomet, Inc. 2 United States USFDA
Zimmer Orthopedic Devices Zimmer Trabecular Metal Technology, Inc. 2 United States USFDA
Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Krupin Eye Valve Ophthalmic Devices Eagle Vision Inc 2 United States USFDA
Depuy Preservation Uni Knee Orthopedic Devices Depuy Orthopaedics, Inc. 3 United States USFDA
Depuy Preservation Uni Knee Orthopedic Devices Depuy Orthopaedics, Inc. 3 United States USFDA
iPulse Circulatory Support System Cardiovascular Devices Abiomed, Inc. 3 United States USFDA
Device Recall SOL SYS L 9IN CALC 2.25/15.0 Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall Free Lock Femoral Fixation System Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall SC2316, Distal Femoral Augment with Screw Orthopedic Devices Stelkast Co 2 United States USFDA
Device Recall Synthes Trochanteric Fixation Nail Orthopedic Devices Synthes USA HQ, Inc. 2 United States USFDA
Device Recall Suture, Nonabsorbable, Synthetic, Polyamide General and Plastic Surgery Devices Teleflex Medical 2 United States USFDA
Device Recall Allez Spine Laguna Pedicle Screw System Orthopedic Devices Allez Spine, LLC 2 United States USFDA
Device Recall KyphX HVR Bone Cement Orthopedic Devices Medtronic Spine LLC, formerly Kyphon Inc 2 United States USFDA
Device Recall SpeedLink 6.0 Transverse Connector Orthopedic Devices Zimmer Inc. 2 United States USFDA
Device Recall Turon Humeral Head Trials Orthopedic Devices Encore Medical, Lp 2 United States USFDA
Superstat Modified Collagen Hemostatic Sponge General and Plastic Surgery Devices Superstat Corp 3 United States USFDA
Zimmer Gender Solutions Natural Knee Flex System, Prolong Articular Surface, Orthopedic Devices Zimmer Inc. 2 United States USFDA
Synthes Spiral Blade Component of the Synthes Modular Blade Plate System Orthopedic Devices Synthes USA (HQ), Inc. 2 United States USFDA