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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall INTERNAL HEX RECON SCREW Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall TRIGEN (TM) LP SCREW, 4.5 MM X 37.5 MM Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall GENESIS(R) II, MOBILE BEARING ARTICULAR INSERT RIGHT Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall REFLECTION(R), MICROSTABLE(R), ACETABULAR LINER Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall Reflection Interfit Shell, 52 MM OD, 3 HOLE Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall TRIGEN(R) INTERTAN(TM) NAIL Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall Reflection, Microstable Acetabular Liner Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall PROMOS Releasing Clamp (3 parts) Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall PROMOS Reverse, Glenosphere Loosening Adapter Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall LEGION Pressfit Stem Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall LEGION Pressfit Stem Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall Oxinium Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall Tandem Unipolar Orthopedic Devices Smith & Nephew Inc 2 United States USFDA
Device Recall PIP FIXATION HINGE Orthopedic Devices Smith & Nephew Inc 2 United States USFDA