CORAILRecalls & reported problems across all models
Depuy (Ireland) · 121 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
CORAIL models — page 2
121 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- CORAIL L971115Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate2 reports
- CORAIL L971213Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 reports
- CORAIL L971311Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- CORAIL L971312Prosthesis, hip, hemi-, femoral, metal2 reports
- CORAIL 3L92520Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- CORAIL 3L93718Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- CORAIL 3L93720Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- CORAIL L20420BROACH1 report
- CORAIL L20500TRAY, SURGICAL, INSTRUMENT1 report
- CORAIL L20504TRAY, SURGICAL, INSTRUMENT1 report
- CORAIL L95680ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- CORAIL L98018Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- CORAIL L98118Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- CORAIL L98511TEMPLATE1 report
- CORAIL L98512TEMPLATE1 report
- CORAIL L98514TEMPLATE1 report
- CORAIL L98520TEMPLATE1 report
- CORAIL L981209Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate1 report
- CORAIL L981310Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate1 report
- CORAIL L971109Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate1 report
- CORAIL L971118Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-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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