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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall NexGen Complete Knee Solution Monoblock Tibial Provisional/Drill Guide Orthopedic Devices Zimmer Trabecular Metal Technology, Inc. 1 United States USFDA
Device Recall ORTHOSENSOR KNEE BALANCER, VERASENSE KNEE SYSTEM Orthopedic Devices Orthosensor, Inc. 2 United States USFDA
Device Recall ATTUNE INTUITION Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Mandible Locking Plate (MLP) Bender / Cutter Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall POWEREASE(TM) Instruments Set Screw Breakoff Instrument Orthopedic Devices Medtronic Sofamor Danek USA Inc 1 United States USFDA
Device Recall Fixed Tibial bearing ATTUNE INTUITION Impactor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Rotating Tibial Platform ATTUNE INTUITION Impactor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Femoral Impactor ATTUNE INTUITION Impactor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall HP LCS IM Hole Locator instrument Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall SpineFrontier PedFuse Pedicle Screw System Orthopedic Devices SpineFrontier, Inc. 1 United States USFDA
Device Recall Synthes Electric Pen Drive (EPD) System Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall Brainlab AG Orthopedic Devices Brainlab AG 2 United States USFDA
Device Recall System 6 Aseptic Housing Orthopedic Devices Stryker Instruments Div. of Stryker Corporation 1 United States USFDA
Device Recall Robotic Arm Interactive Orthopedic System (RIO) Orthopedic Devices Mako Surgical Corporation 2 United States USFDA
Device Recall KYPHON(R) EXPRESS(TM), Osteo Introducer(R) System, Diamond and Bevel, Size 2 Orthopedic Devices Medtronic Sofamor Danek USA Inc 1 United States USFDA
Device Recall Synthes Inserter for Titanium Elastic Nails Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall RECLAIM Revision Hip System; Assembled Implant Inserter Adaptor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Reamers Orthopedic manual surgical instrument Orthopedic Devices Captiva Spine, Inc 1 United States USFDA
Device Recall Instrument Kit for use with OsteoSponge SC grafts Orthopedic Devices Bacterin International, Inc. 1 United States USFDA
Device Recall Lineum HF Torque Handle Limit (Lineum) Orthopedic Devices Biomet Spine, LLC 1 United States USFDA
Device Recall Torque Limiting Handle (Aspen/ Alpine) Orthopedic Devices Biomet Spine, LLC 1 United States USFDA
Device Recall Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 Orthopedic Devices The Anspach Effort, Inc. 1 United States USFDA
Device Recall Stryker Instruments Orthopedic Devices Stryker Instruments Div. of Stryker Corporation 1 United States USFDA
Device Recall Zimmer Anatomical Shoulder Handle for Rasp Orthopedic Devices Zimmer Gmbh 1 United States USFDA
Device Recall Cannulated Drill Bits Orthopedic Devices Synthes, Inc. 1 United States USFDA