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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall NEXGEN COMPLETE KNEE SOLUTION LEGACY POSTERIOR STABILIZED (LPS); LPSFLEX FIXED BEARING FEMORAL AND Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall NEXGEN KNEE PROSTHESIS & LEGACY KNEE PROSTHESIS W/CONIDIUM SURFACE HARDENING PROCESS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall AccuLIF Tubing Set Orthopedic Devices Stryker Spine 2 United States USFDA
Device Recall NEXGEN COMPL. KNEE SOL. LEGACY POSTERIOR STABILIZED/CONSTRAINED CONDYLAR KNEE FEMORAL COMPONENTS/ART Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall NEXT GENERATION KNEE SYSTEM Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall ZIMMER UNICOMPARTMENTAL KNEE SYSTEM Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall ZIMMER PATELLOFEMORAL JOINT PROSTHESIS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall GENDER SOLUTIONS NATURALKNEE FLEX SYSTEM; NEX GEN COMPLETE KNEE SOLUTION CRFLEX GENDER SOLUTIONS F Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall NATURALKNEE II SYSTEM Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall NEXGEN COMPLETE KNEE SOLUTION LPSFLEX AND KNEE GENDER SOLUTIONS FEMALE (GSF) POROUS FEMORAL COMPONE Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall ZIMMER NEXGEN LPSFLEX MOBILE AND LPS MOBILE BEARING KNEE SYSTEM Orthopedic Devices Zimmer Biomet, Inc. 3 United States USFDA
Device Recall NexGen Complete Knee Solution MIS Total Knee Procedure Cruciate Retaining CR Flex Mobile Bearing Pre Orthopedic Devices Zimmer Biomet, Inc. 3 United States USFDA
Device Recall CPT 12/14 HIP PROSTHESES, MODEL 008114040/05000 Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall COLLARLESS POLISHED TAPER HIP PROSTHESIS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall BIPOLAR HIP DEVICE Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall VERSYS HIP SYSTEM BEADED MIDCOAT LOW HEAD CENTER HIP PROSTHESIS, MODEL 007840XXXXX Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall VERSYS BEADED FULLCOAT BOWED REVISION HIP PROSTHESIS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall VERSYS HIP SYSTEM BEADED HIP PROSTHESIS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall BETA HIP PROSTHESIS Orthopedic Devices Zimmer Biomet, Inc. 2 United States USFDA
Device Recall METASUL TAPER LINERS, METASUL FEMORAL HEADS Orthopedic Devices Zimmer Biomet, Inc. 3 United States USFDA
Device Recall GAM Guide/Metaizeau Intramedullary Pin Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Guide Wires and KWires for T2 and Gamma System Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Guide and KWires for T2 and Gamma Systems Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Guide and KWires for T2 and Gamma Systems Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Guide and KWires for T2 and Gamma Systems Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA