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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall EVOLUTION MP TIBIAL BASE, REF ETPKN8SR Orthopedic Devices Microport Orthopedics INC. 2 United States USFDA
Device Recall PROFEMUR(R) R RASP HANDLE Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Cobalt Chromium Heads Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Conserve Cups Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Conserve Shells Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Lineage Shell Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Procotyl (Rim Lock) Liners Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Dynasty Liners Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall Lineage Liners Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
Device Recall PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK Orthopedic Devices MicroPort Orthopedics Inc. 2 United States USFDA
femoral neck component Orthopedic Devices MicroPort Orthopedics Germany BAM
CONSERVE Shell, DYNASTY Metal Liner, PROCOTYL Metal Liner and LINEAGE Metal Liner MicroPort Orthopedics Germany BAM
EVOLUTION® Tibial Base MicroPort Orthopedics Germany BAM
PROFEMUR PLUS CoCr MODULAR NECK PHAC1254 Orthopedic Devices MicroPort Orthopedics, Inc. 2 United States USFDA