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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Trilogy Bone Screws Orthopedic Devices Zimmer Manufacturing B.V. 2 United States USFDA
Device Recall Conformis iTotal CR G2 Knee Replacement System Orthopedic Devices ConforMIS, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall Osteobond Copolymer Bone Cement Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Persona Cemented Tibial Broach Inserter/Extractor Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Sirius Polish Cemented Stem 34B Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Sirius Polish Cemented Stem 34B Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall SolitaireC Cervical Spacer System Orthopedic Devices Ebi, Llc 2 United States USFDA
Device Recall BIOLOX delta TS Ceramic Femoral Head Articul/eze 12/14 36mm 12 Orthopedic Devices DePuy Orthopaedics, Inc. 2 United States USFDA
Device Recall TiBond Orthopedic Devices Spinal Elements, Inc 2 United States USFDA
Device Recall Timberline Anchored Lateral Retractable Drill Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Anchored Lateral Variable Retractable Sleeve Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Anchored Lateral Retractable Sleeve Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall EXp Tibial Insert Orthopedic Devices Stelkast Co 2 United States USFDA
Device Recall Stryker Orthopedics Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Zimmer PERSONA Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall PERSONA Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Howmedica Osteonics Corp. LFT v40 Femoral Head Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Stryker Howmedica Osteonics Triathlon Distal Capture Assembly Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Telluride Percutaneous Rod Inserter Long Orthopedic Devices Biomet Spine, LLC 2 United States USFDA