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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall DePuy Orthopaedics LCS COMPLETE RPS Orthopedic Devices DePuy Orthopaedics, Inc. 3 United States USFDA
Device Recall Construx Alum Ankle Clamp Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Orthopedic Devices Zimmer, Inc. 3 United States USFDA
Device Recall 3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws Orthopedic Devices Synthes, Inc. 2 United States USFDA
Device Recall Rod and screw spinal instrumentation Orthopedic Devices Orthofix, 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 CONSTRAINED LINER Orthopedic Devices Smith & Nephew, Inc. 2 United States USFDA
Device Recall DePuy Synthes Titanium Recon Screws Orthopedic Devices Synthes, Inc. 2 United States USFDA
Device Recall Apex ARC Hip Stem Orthopedic Devices Omnilife Science Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall A.L.P.S. Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall ATTUNE" Articulation Surface Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall Rotate, BulletTip, TPlus, Contact, Crossfuse, and CrossFuse II, Interbody Fusion/Vertebral Body Re Orthopedic Devices RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) 2 United States USFDA
Device Recall TITANIUM END CAP WITH T40 STARDRIVE RECESS, 0MM EXTENSION FOR TITANIUM TIBIAL NAILSEX Orthopedic Devices Synthes, Inc. 2 United States USFDA