EMPHASYSRecalls & reported problems across all models
Depuy (Ireland) · 109 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
EMPHASYS models — page 2
109 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- EMPHASYS 4800-70-050TRAY, SURGICAL, INSTRUMENT1 report
- EMPHASYS 4830-40-028TEMPLATE1 report
- EMPHASYS 4830-42-028TEMPLATE1 report
- EMPHASYS 4830-48-028TEMPLATE1 report
- EMPHASYS 4817-00-090Orthopedic manual surgical instrument1 report
- EMPHASYS 4825-52-042TEMPLATE1 report
- EMPHASYS 4732-46-036Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- EMPHASYS 4732-48-028PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- EMPHASYS 4732-52-028PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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