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.
- ARCOS 3.5MM HEX DRIVER W/O HUDSON 31-301880SCREWDRIVER1 report
- OSS™ Orthopedic Salvage System 151806PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OSS™ Orthopedic Salvage System 151855PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Vanguard Knee System 189043Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Vanguard Knee System 189063PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Vanguard Knee System 189081PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Vanguard Knee System 189083PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Vanguard Knee System 189103Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- OSS™ Orthopedic Salvage System 151838PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OSS™ Orthopedic Salvage System 151844PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- VANGUARD TIBIAL BEARING TRIAL ANTERIOR STABILIZED 32-489043PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- VANGUARD TIBIAL BEARING TRIAL ANTERIOR STABILIZED 32-489061PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- COMPREHENSIVE REVERSE SHOULDER 115393prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 report
- JuggerLoc Bone to Bone 110007337WASHER, BOLT NUT1 report
- POSITIONING GUIDE ADAPTOR ROD 110024515ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Comprehensive Reverse Shoulder TI-115313PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- Comprehensive Reverse Shoulder TI-115320prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 report
- G7 EFFICIENT INSTRUMENT TRAY 110025612TRAY, SURGICAL, INSTRUMENT1 report
- Arcos® One-piece Revision System 11-304014Prosthesis, hip, hemi-, femoral, metal1 report
- G7® Dual Mobility Acetabular System 110024459Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193009Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193011Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193012Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193014Prosthesis, hip, hemi-, femoral, metal1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193015Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193017Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193018Prosthesis, hip, hemi-, femoral, metal1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193021Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193110Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193117Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- Orthopedic Salvage System (OSS™) CP114842PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- 1 report
- G7® Dual Mobility 110024732Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Arcos® One-piece Revision System 110024782ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- COMPREHENSIVE INSTRUMENTATION 110028878PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- COMPREHENSIVE® INSTRUMENTATION 110025762shoulder prosthesis, reverse configuration1 report
- Dual Mobility 110030158ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Dual Mobility 110030153ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Dual Mobility 110030155ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Dual Mobility 110030159ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- COMPREHENSIVE® SRS / NEXEL 110029826PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- COMPREHENSIVE® SRS / NEXEL 110029938PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- Persona® Partial Knee System 42-5580-002-02PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- COMPREHENSIVE® REVERSE SHOULDER 110040420prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented1 report
- DVR® CROSSLOCKPLATE LEFT (HEAD WIDTH X OVERALL LENGTH) 1318-22-051APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE1 report
- Persona® Partial Knee System 42-5380-003-02PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5380-009-01PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5380-009-02PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- DVR® CROSSLOCKVOLAR RIM PLATE 131814051APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE1 report
- Persona® Partial Knee System 42-5182-003-09PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-003-10PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-003-12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5282-003-08PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-004-09PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-004-10PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-004-11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5282-004-08PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5282-004-10PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-005-11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-006-10PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-006-12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-007-09PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-007-10PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5182-008-08PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5282-008-08PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Persona® Partial Knee System 42-5282-008-10PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Comprehensive® VRS Glenoid 110019066shoulder prosthesis, reverse configuration1 report
- BI-AXIAL™ ELBOW SYSTEM CP562351Prosthesis, Elbow, Constrained, Cemented1 report
- COMPREHENSIVE® VRS INSTRUMENT 110028045shoulder prosthesis, reverse configuration1 report
- COMPREHENSIVE® VRS 110019063shoulder prosthesis, reverse configuration1 report
- A.L.P.S.® CLAVICLE PLATING SYSTEMCLAVICLE DEPTH GAUGE 233500003Plate, fixation, bone1 report
- OSS™ Orthopedic Salvage System CP113462PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Comprehensive® SRS / Discovery® 211254PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- Comprehensive® SRS 110029940PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 report
- JUGGERKNOT® 912071Fastener, fixation, nondegradable, soft tissue1 report
- G7 LATERAL POSITIONING GUIDE 110003456TISSUE GRAFT OF LESS THAN 6MM1 report
- JUGGERKNOT LONG 110016992Fastener, fixation, nondegradable, soft tissue1 report
- Vanguard® Complete Knee System 195543PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Vanguard® Complete Knee System 195610Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- M2a Magnum™ Hip System US157846PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- M2a Magnum™ Hip System US157850PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- BONE SCREW, CORTICAL 14377-16Screw, fixation, bone1 report
- PEG SCREW 1312-12-520PIN, FIXATION, THREADED1 report
- PEG SCREW 1312-12-526APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT1 report
- DISTAL HUMERAL POST LATERAL PLATE, LEFT LARGE 1312-18-303WASHER, BOLT NUT1 report
- Locked Plate, T-Shape Small 1312-20-157WASHER, BOLT NUT1 report
- LOCKING SCREW 1312-20-416Screw, fixation, bone1 report
- LOCKING SCREW 1312-20-418PIN, FIXATION, SMOOTH1 report
- LOCKING SCREW 1312-20-420PIN, FIXATION, THREADED1 report
- NON-LOCKING SCREW 1312-20-522PLATE, FIXATION, BONE1 report
- VERSANAIL®UNIVERSAL HUMERAL NAIL 1817-08-241ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES1 report
- 1 report
- 130 DEGREE INSERTION JIG 2112-01-201ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- LAG SCREW DRILL 2112-01-303STARTER, BONE SCREW1 report
- LAG SCREW COUPLING ROD 2112-01-306ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- LAG SCREW DRIVER 2112-01-307SCREWDRIVER1 report
- DISTAL GRADUATED DRILL LONG 2112-01-405BIT, DRILL1 report
- ANTI-ROTATION SCREW DRILL 2112-01-505BIT, DRILL1 report
- T-15 TAPERED DRIVER 2142-15-070DRIVER, PROSTHESIS1 report
- A.L.P.S.CALIBRATED DRILL 2142-27-160BIT, DRILL1 report