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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Cannulated Drill Bit Orthopedic Devices Trilliant Surgical Ltd. 1 United States USFDA
Device Recall Reamer Head Orthopedic Devices Trilliant Surgical Ltd. 1 United States USFDA
Device Recall ARHTROSCOPY PK L/F Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Aliquot Delivery Kit (Syringe and Plunger) Orthopedic Devices Orthovita, Inc., dBA Stryker Orthobiologics. 1 United States USFDA
Device Recall ConFormis Orthopedic Devices ConforMIS, Inc. 2 United States USFDA
Device Recall ConForMis Orthopedic Devices ConforMIS, Inc. 2 United States USFDA
Device Recall ConforMIS Orthopedic Devices ConforMIS, Inc. 2 United States USFDA
Device Recall Robotic Arm Interactive Orthopedic System Orthopedic Devices Mako Surgical Corporation 2 United States USFDA
Device Recall FMS neXtra 3.5mm Full Radius Cutter Shaver Blades Orthopedic Devices DePuy Mitek, Inc., a Johnson & Johnson Co. 2 United States USFDA
Device Recall FMS neXtra 3.5mm Aggressive Cutter Shaver Blades Orthopedic Devices DePuy Mitek, Inc., a Johnson & Johnson Co. 2 United States USFDA
Device Recall FMS 3.5mm UltraAggressive Cutter Shaver Blades Orthopedic Devices DePuy Mitek, Inc., a Johnson & Johnson Co. 2 United States USFDA
Device Recall Persona EM Proximal Tube Orthopedic Devices Zimmer, Inc. 1 United States USFDA
Device Recall Persona EM Distal Rod Orthopedic Devices Zimmer, Inc. 1 United States USFDA
Device Recall Endoscopic Tarsal Tunnel Decompression Orthopedic Devices Instratek, Incorporated 2 United States USFDA
Device Recall Synthes Orthopedic Devices Synthes (USA) Products LLC 1 United States USFDA
Device Recall Biomet Black Mamba Suture Passer Orthopedic Devices Biomet, Inc. 1 United States USFDA
Device Recall Biomet Green Mamba Suture Passer Orthopedic Devices Biomet, Inc. 1 United States USFDA
Device Recall smith & nephew Orthopedic Devices Smith & Nephew, Inc., Endoscopy Div. 1 United States USFDA
Device Recall Firebird Spinal Fixation System Orthopedic Devices Orthofix, Inc 1 United States USFDA
Device Recall Smith & Nephew Orthopedic Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Richard Wolf Medical Istruments Orthopedic Devices Richard Wolf Medical Instruments Corp. 2 United States USFDA
Device Recall Richard Wolf Medical Istruments Orthopedic Devices Richard Wolf Medical Instruments Corp. 2 United States USFDA
Device Recall Richard Wolf Medical Istruments Orthopedic Devices Richard Wolf Medical Instruments Corp. 2 United States USFDA
Device Recall Stryker Spine Orthopedic Devices Stryker Spine 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA