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Nom Classification Fabricant Classe de risque Pays Source
Synex II Modular Vertebral Body Replacement System Orthopedic Devices Synthes Germany BAM
femoral neck component Orthopedic Devices MicroPort Orthopedics Germany BAM
the Oasys Midline Plates Orthopedic Devices STRYKER Germany BAM
Comprehensive Reverse Shoulder Tray Orthopedic Devices Zimmer Biomet Germany BAM
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 Trilogy Bone Screws Orthopedic Devices Zimmer Manufacturing B.V. 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 TiBond Orthopedic Devices Spinal Elements, Inc 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