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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Biomet Integral Centralizer Hip System Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Orthopedic Devices Orthopedic Devices Synthes (USA) Products LLC 2 United States USFDA
Device Recall Trochanteric Fixation Nail Advanced System Orthopedic Devices Synthes (USA) Products LLC 2 United States USFDA
Device Recall MODEL: Aegis Torque Handle CATALOG NO. : 287110800 Orthopedic Devices DePuy Spine, Inc. 2 United States USFDA
Device Recall Arthrosurface ToeMotion" Orthopedic Devices Arthrosurface, Inc. Unclassified United States USFDA
Device Recall I.B.S. orthosynthesis screws Orthopedic Devices In2Bones, SAS 2 United States USFDA
Device Recall BIRMINGHAM HIP RESURFACING MODULAR HEAD Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall Zimmer NexGen Precoat Stemmed Tibia Orthopedic Devices Zimmer Manufacturing B.V. 2 United States USFDA
Device Recall NexGen Precoat Stemmed Tibia/NexGen Nonaugmentable Tibial Component Orthopedic Devices Zimmer Manufacturing B.V. 2 United States USFDA
Device Recall Biomet A.L.P.S. 4.0mm Cancellous Locking Screws Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Trial Shell component of the accessory kit to the Shoulder Prosthesis Stem Orthopedic Devices Encore Medical, Lp 2 United States USFDA
Device Recall Zimmer, Virage OCT Spinal Fixation System Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall B. Braun AM Aesculap Orthopedic Devices Aesculap, Inc. 2 United States USFDA
Device Recall GENESIS II/LEGION Resurfacing Patella with JOURNEY Peg Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall Excella II Rod Orthopedic Devices Innovasis, Inc 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Manufacturing B.V. 2 United States USFDA
Device Recall Zimmer Periarticular Locking Plate System Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall Zimmer Universal Locking System Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall Response 5.5/6.0 Spine System Orthopedic Devices OrthoPediatrics Corp 2 United States USFDA
Device Recall Stryker Vitallium Wire (6 Pack) Non Sterile Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall DVR ePAK Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall NEXGEN KNEE GENDER SOLUTIONS FEMALE (GSF) FEMORAL COMPONENTS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall Guide Wires and KWires for T2 and Gamma Systems Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall LEGION Hemi Stepped Tibial Wedge Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall NEXGEN COMPLETE KNEE SOLUTION CRUCIATE RETAINING (CR)FLEX FEMORAL COMPONENTS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA