INSTRUMENTRecalls & reported problems across all models
Howmedica Osteonics Corp. · 131 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
INSTRUMENT models — page 2
131 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- INSTRUMENT 6264-8-236RProsthesis, hip, semi-constrained, uncemented, metal/polymer, porous1 report
- INSTRUMENT 5650-4-512ABIT, DRILL1 report
- INSTRUMENT 1020-5200Screw, fixation, bone1 report
- INSTRUMENT 1020-5208Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 report
- INSTRUMENT 1020-5207Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- INSTRUMENT 7650-2038AORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- INSTRUMENT I-K2710KB00PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT I-K2958TI00ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- INSTRUMENT I-H1551HF00Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish1 report
- INSTRUMENT I-H1417RS00Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- INSTRUMENT I-K34960709PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT I-K34960713PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- INSTRUMENT I-K34960411PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT I-K2869KF00Guide, surgical, instrument1 report
- INSTRUMENT I-K1985DS00PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT I-K2291KB00ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- INSTRUMENT 7004-0100IMPACTOR1 report
- INSTRUMENT 5530-T-509YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5530-T-711YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5531-T-609YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5532-T-509YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5532-T-409YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5530-T-411YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5530-T-309YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5530-T-310YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5530-T-109YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5531-T-111YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5531-T-110YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5532-T-214YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5531-T-509YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- INSTRUMENT 5531-T-209YPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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