S-ROMRecalls & reported problems across all models
Depuy (Ireland) · 185 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
S-ROM models — page 2
185 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- S-ROM 1365-65-500Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- S-ROM 2576-04-016INSTRUMENT, CUTTING, ORTHOPEDIC2 reports
- S-ROM 2576-04-018INSTRUMENT, CUTTING, ORTHOPEDIC2 reports
- S-ROM 2576-05-025TEMPLATE2 reports
- S-ROM 2576-11-102TEMPLATE2 reports
- S-ROM 2576-14-105TEMPLATE2 reports
- S-ROM 2576-24-100TEMPLATE2 reports
- S-ROM 52-3208Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented2 reports
- S-ROM 52-3251Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented2 reports
- S-ROM 52-3395Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented2 reports
- S-ROM 53-4312DRIVER, PROSTHESIS2 reports
- S-ROM 53-4320DRIVER, PROSTHESIS2 reports
- S-ROM 53-4712REAMER2 reports
- S-ROM 53-5506REAMER2 reports
- S-ROM 53-5508REAMER2 reports
- S-ROM 53-6316TEMPLATE2 reports
- S-ROM 53-6330TEMPLATE2 reports
- S-ROM 53-6809REAMER2 reports
- S-ROM 53-6813REAMER2 reports
- S-ROM 53-6814REAMER2 reports
- S-ROM 53-6851REAMER2 reports
- S-ROM 53-6859REAMER2 reports
- S-ROM 54-0002REAMER2 reports
- S-ROM 54-0004REAMER2 reports
- S-ROM 87-5917TEMPLATE2 reports
- S-ROM 87-5926TEMPLATE2 reports
- S-ROM 87-5927TEMPLATE2 reports
- S-ROM 87-5962TEMPLATE2 reports
- S-ROM 1365-35-000PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- S-ROM 1365-61-500PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- S-ROM 2365-34-500TEMPLATE1 report
- S-ROM 2576-00-006BIT, DRILL1 report
- S-ROM 2576-09-102TEMPLATE1 report
- S-ROM 2576-09-104TEMPLATE1 report
- S-ROM 2576-11-104TEMPLATE1 report
- S-ROM 2576-12-100TEMPLATE1 report
- S-ROM 2576-13-020ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- S-ROM 2576-14-009TEMPLATE1 report
- S-ROM 2576-14-110TEMPLATE1 report
- S-ROM 2576-14-115TEMPLATE1 report
- S-ROM 2576-14-120TEMPLATE1 report
- S-ROM 2576-14-125TEMPLATE1 report
- S-ROM 2576-16-011TEMPLATE1 report
- S-ROM 2576-17-102TEMPLATE1 report
- S-ROM 2576-17-104TEMPLATE1 report
- S-ROM 2576-18-013TEMPLATE1 report
- S-ROM 2576-19-100TEMPLATE1 report
- S-ROM 2576-20-015TEMPLATE1 report
- S-ROM 2576-21-100TEMPLATE1 report
- S-ROM 2576-22-105TEMPLATE1 report
- S-ROM 2576-22-120TEMPLATE1 report
- S-ROM 2576-22-125TEMPLATE1 report
- S-ROM 2576-24-105TEMPLATE1 report
- S-ROM 2576-24-110TEMPLATE1 report
- S-ROM 2576-24-115TEMPLATE1 report
- S-ROM 2576-24-125TEMPLATE1 report
- S-ROM 52-3195Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented1 report
- S-ROM 52-3396Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented1 report
- S-ROM 53-1205EXTRACTOR1 report
- S-ROM 53-2997EXTRACTOR1 report
- S-ROM 53-2999EXTRACTOR1 report
- S-ROM 53-4149ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- S-ROM 53-4151ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- S-ROM 53-4322DRIVER, PROSTHESIS1 report
- S-ROM 53-4516EXTRACTOR1 report
- S-ROM 53-4520EXTRACTOR1 report
- S-ROM 53-4522EXTRACTOR1 report
- S-ROM 53-4700REAMER1 report
- S-ROM 53-4702REAMER1 report
- S-ROM 53-4714REAMER1 report
- S-ROM 53-6322TEMPLATE1 report
- S-ROM 53-6348TEMPLATE1 report
- S-ROM 53-6350TEMPLATE1 report
- S-ROM 53-6810REAMER1 report
- S-ROM 53-6812REAMER1 report
- S-ROM 53-6815REAMER1 report
- S-ROM 53-6816REAMER1 report
- S-ROM 53-6850REAMER1 report
- S-ROM 53-6852REAMER1 report
- S-ROM 53-6853REAMER1 report
- S-ROM 53-6855REAMER1 report
- S-ROM 54-0003REAMER1 report
- S-ROM 54-0005REAMER1 report
- S-ROM 87-5930TEMPLATE1 report
- S-ROM 87-5960TEMPLATE1 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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