Biomet Orthopedics, LLC
2,125 devices · 8,768 adverse event reports · 27 deaths reported · 495 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
Biomet Orthopedics, LLC products
- AFFIXUSHIP FRACTURE NAIL - RIGHT39 models · 6 reports · 37 recalls
- AFFIXUSHIP FRACTURE NAIL - LEFT27 models · 7 reports · 24 recalls
- Compress Device71 models · 99 reports · 22 recalls
- Arcos Modular Revision Hip System71 models · 191 reports · 19 recalls
- Comprehensive Reverse Shoulder57 models · 895 reports · 3 recalls
- Vanguard Knee System147 models · 306 reports · 13 recalls
- STAGEONE17 models · 0 reports · 18 recalls
- StageOne Select15 models · 2 reports · 15 recalls
- Comprehensive Shoulder System68 models · 191 reports · 11 recalls
- Taperloc Complete Primary Femoral40 models · 733 reports
- Taperloc Complete Micro Primary Femoral35 models · 679 reports
- JuggerStitch4 models · 454 reports
- COMPREHENSIVE INSTRUMENTATION18 models · 413 reports
- G7 Acetabular System42 models · 352 reports · 1 recall
- G7 Acetabular Liner85 models · 358 reports
- JuggerKnot Soft Anchors15 models · 301 reports · 1 recall
- Intramedullary Bone Saw7 models · 0 reports · 7 recalls
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL15 models · 297 reports
- TAPERLOC COMPLETE XR 123 FEMORAL15 models · 275 reports
- RINGLOC BI-POLAR HIP SYSTEM16 models · 100 reports · 3 recalls
- OSS Orthopedic Salvage System76 models · 181 reports · 1 recall
- AFFIXUSHIP FRACTURE NAIL4 models · 5 reports · 4 recalls
- RingLoc Hip System40 models · 53 reports · 3 recalls
- Persona Partial Knee System60 models · 201 reports
- Biomet Knee System72 models · 137 reports · 1 recall
- G7 Dual Mobility Acetabular System8 models · 119 reports · 1 recall
- Biomet Hip System37 models · 115 reports · 1 recall
- Hybrid Glenoid4 models · 51 reports · 2 recalls
- A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMHIGH PLATE RIGHT3 models · 0 reports · 3 recalls
- Gentle Threads8 models · 17 reports · 2 recalls
- LOCK SCREW SQUARE DRIVE5 models · 8 reports · 2 recalls
- BALL NOSE GUIDE WIRE3 models · 4 reports · 2 recalls
- Oxford Partial Knee System10 models · 4 reports · 2 recalls
- A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMHIGH PLATE LEFT4 models · 2 reports · 2 recalls
- A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE RIGHT3 models · 1 reports · 2 recalls
- BIOMET PATELLAR SYSTEM2 models · 0 reports · 2 recalls
- Echo Bi-Metric Hip System35 models · 50 reports · 1 recall
- BI-METRIC X-SERIES HIP SYSTEM27 models · 0 reports · 2 recalls
- DFS HA BONE SCREWS52 models · 0 reports · 2 recalls
- JuggerLoc2 models · 0 reports · 2 recalls
- G7 ACETABULAR SCREW9 models · 95 reports
- Flexible Silicone Drill Driver2 models · 94 reports
- EXPLOR15 models · 42 reports · 1 recall
- ZIPTIGHT FIXATION SYSTEM4 models · 42 reports · 1 recall
- ORTHOPEDIC SALVAGE SYSTEM (OSS)8 models · 40 reports · 1 recall
- Active Articulation Hip System9 models · 83 reports
- ARCOS MODULAR REVISION SYSTEM14 models · 71 reports
- Regenerex6 models · 18 reports · 1 recall
- Modular Arthrodesis Nail6 models · 14 reports · 1 recall
- G7 OSSEOTI ACETABULAR SHELL18 models · 62 reports
- ZIPTIGHT2 models · 10 reports · 1 recall
- Active Articulation Dual Mobility Hip System5 models · 7 reports · 1 recall
- BIO-MODULAR SHOULDER SYSTEM9 models · 6 reports · 1 recall
- DRILL BIT3 models · 5 reports · 1 recall
- TAPERLOC HIP SYSTEM22 models · 4 reports · 1 recall
- VANGUARD 360 REVISION SYSTEM4 models · 3 reports · 1 recall
- Vanguard M Partial Knee System20 models · 3 reports · 1 recall
- PEG FULLY THREADED, LOCKING3 models · 2 reports · 1 recall
- MALLORY/HEAD PRIMARY HIP SYSTEM20 models · 2 reports · 1 recall
- DVR CROSSLOCK5 models · 2 reports · 1 recall
All Biomet Orthopedics, LLC devices
- JuggerStitch® 110024773Fastener, fixation, nondegradable, soft tissue397 reports
- Comprehensive Reverse Shoulder 010000589PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- COMPREHENSIVE INSTRUMENTATION 110029132PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED116 reports
- Arcos Modular Revision Hip System 11-301301Prosthesis, hip, semi-constrained, metal/polymer, cemented2 recalls8 reports
- JuggerKnot Soft Anchors 912082FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE107 reports
- VANGUARD KNEE SYSTEM 184764PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 recalls5 reports
- COMPREHENSIVE SHOULDER SYSTEM 113633PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED2 recalls4 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165206Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 recalls3 reports
- Vanguard® Knee System 183108PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 recalls3 reports
- Vanguard® Knee System 183126PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 recalls3 reports
- Comprehensive® Instrumentation 110029132PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED103 reports
- Vanguard® Knee System 189082PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 recalls2 reports
- Compress® Device 178562PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls2 reports
- STAGEONE 431209Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 recalls0 reports
- STAGEONE 431207Prosthesis, hip, hemi-, femoral, metal2 recalls0 reports
- DFS HA BONE SCREWS HAA60-11030APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-12040Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAA60-13040APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15030APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15020APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15040APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15050APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15060APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-18030APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-18060Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAA60-18040APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-20030Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAA60-20060Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAA60-22050Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAA60-25050Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAB60-11050Screw, fixation, bone2 recalls0 reports
- DFS HA BONE SCREWS HAB60-12040APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- Compress® Device 178754shoulder prosthesis, reverse configuration2 recalls0 reports
- Comprehensive Reverse Shoulder 115310prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 death99 reports
- Taperloc Complete Micro Primary Femoral 51-107170Prosthesis, hip, semi-constrained, metal/polymer, cemented83 reports
- G7® Acetabular System 010000663Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall30 reports
- Comprehensive® Reverse Shoulder 115395PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall1 death25 reports
- ZIPTIGHT FIXATION SYSTEM 904759FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE1 recall23 reports
- G7® Dual Mobility Acetabular System 110024462Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall22 reports
- COMPREHENSIVE INSTRUMENTATION 110028879shoulder prosthesis, reverse configuration71 reports
- FLEXIBLE SILICONE DRILL DRIVER 110010733BIT, DRILL65 reports
- Hybrid Glenoid 113954PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall13 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165228Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall1 death12 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165218PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall2 deaths9 reports
- Compress® Device 178552Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- Arcos Modular Revision Hip System 11-301310Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish1 recall9 reports
- ZIPTIGHT 904834FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145170Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented59 reports
- A.L.P.S.® 2142-27-160BIT, DRILL1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145160PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED58 reports
- Gentle Threads 905612Screw, fixation, bone1 recall7 reports
- Arcos Modular Revision Hip System 11-301321PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall7 reports
- Arcos Modular Revision Hip System 11-301300Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall7 reports
- Comprehensive® Reverse Shoulder XL-115364prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 recall7 reports
- Taperloc Complete Primary Femoral 51-104170Prosthesis, hip, semi-constrained, metal/polymer, cemented56 reports
- Compress® Device 178366Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall6 reports
- JuggerKnot Soft Anchors 912076FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE56 reports
- Compress® Device 178404Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall5 reports
- Vanguard® Knee System 183620PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall5 reports
- Compress® Device 178554Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall5 reports
- Arcos Modular Revision Hip System 11-301311Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall5 reports
- Arcos Modular Revision Hip System 11-301302PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall5 reports
- Compress® Device 178354Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall5 reports
- Regenerex 141356Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer1 recall5 reports
- RingLoc® Hip System 103533Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall4 reports
- Vanguard® Knee System 183106PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall4 reports
- Compress® Device 178556Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall4 reports
- Compress® Device 178558PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall4 reports
- Arcos Modular Revision Hip System 11-301312Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall4 reports
- Arcos Modular Revision Hip System 11-300814Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall4 reports
- Arcos Modular Revision Hip System 11-301342Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish1 recall4 reports
- Arcos Modular Revision Hip System 11-301331Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall4 reports
- Comprehensive® Reverse Shoulder XL-115366prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 recall4 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented54 reports
- G7 DEPTH GAUGE 110010717Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented54 reports
- BIOMET KNEE SYSTEM 141215Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer1 recall3 reports
- OSS™ Orthopedic Salvage System 150414PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall3 reports
- Compress® Device 178406Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall3 reports
- Vanguard® Knee System 183104PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall3 reports
- Vanguard® Knee System 183122PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall3 reports
- VANGUARD KNEE SYSTEM 184762PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall3 reports
- VANGUARD KNEE SYSTEM 184766PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall3 reports
- Arcos Modular Revision Hip System 11-301333Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall3 reports
- Taperloc Complete Primary Femoral 51-104150Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate53 reports
- Compress® Device 178367PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall3 reports
- Compress® Device 178364Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall3 reports
- JUGGERKNOT SOFT ANCHORS 912068FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE53 reports
- Taperloc Complete Micro Primary Femoral 51-106150Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented53 reports
- JuggerKnot Soft Anchors 912080FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE1 recall3 reports
- G7® Acetabular System 010000667PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall3 reports
- BALL NOSE GUIDE WIRE 2810-01-100Guide, surgical, instrument1 recall3 reports
- DRILL BIT 212000022BIT, DRILL1 recall3 reports
- A.L.P.S.® 8290-29-170BIT, DRILL1 recall3 reports
- BIOMET HIP SYSTEM 11-363660PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall2 reports
- Compress® Device 178400PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall2 reports
- Compress® Device 178402PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall2 reports
- Vanguard® Knee System 183124PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall2 reports
- Hybrid Glenoid 113956PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall2 reports
- COMPREHENSIVE SHOULDER SYSTEM 113629PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall2 reports
- COMPREHENSIVE SHOULDER SYSTEM 113631PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall2 reports