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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall CONSTRAINED LINER Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall CONSTRAINED LINER Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall CONSTRAINED LINER Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall CONSTRAINED LINER Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall CONSTRAINED LINER Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD, Orthopedic Devices Smith & Nephew, Inc. 3 United States USFDA
Device Recall Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR Orthopedic Devices Smith & Nephew, Inc. 3 United States USFDA
Device Recall Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR Orthopedic Devices Smith & Nephew, Inc. 3 United States USFDA
Device Recall BIRMINGHAM HIP RESURFACING MODULAR HEAD Orthopedic Devices Smith & Nephew, 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 LEGION Hemi Stepped Tibial Wedge Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall TCPLUS(TM), Primary Fixed Tibial Component VKS Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA