REFLECTIONRecalls & reported problems across all models
Smith & Nephew, Inc. · 112 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
REFLECTION models — page 2
112 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- REFLECTION 71333347PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- REFLECTION 71363655Prosthesis, hip, femoral component, cemented, metal1 report
- REFLECTION 71363656Prosthesis, hip, femoral component, cemented, metal1 report
- REFLECTION 71333435Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- REFLECTION 71362635Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- REFLECTION 71335154PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- REFLECTION 71335158PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- REFLECTION 71363252Prosthesis, hip, femoral component, cemented, metal1 report
- REFLECTION 71333447PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- REFLECTION 71362109ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REFLECTION 71363258Prosthesis, hip, femoral component, cemented, metal1 report
- REFLECTION 71333495PROSTHESIS, 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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