RECLAIMRecalls & reported problems across all models
Depuy (Ireland) · 149 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
RECLAIM models — page 2
149 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- RECLAIM 1975-28-105Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1976-15-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1976-19-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-17-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-18-240Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-19-240Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-21-290Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-22-240Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-23-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-25-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-27-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1977-27-290Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 2975-00-625ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RECLAIM 2975-00-645ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RECLAIM 2975-00-755ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- RECLAIM 2975-24-105REAMER1 report
- RECLAIM 2976-14-190REAMER1 report
- RECLAIM 2976-15-190REAMER1 report
- RECLAIM 2976-16-190REAMER1 report
- RECLAIM 2976-16-240REAMER1 report
- RECLAIM 2976-17-190REAMER1 report
- RECLAIM 2976-17-240REAMER1 report
- RECLAIM 2976-18-190REAMER1 report
- RECLAIM 2976-18-240REAMER1 report
- RECLAIM 2976-19-190REAMER1 report
- RECLAIM 2976-19-240REAMER1 report
- RECLAIM 2976-20-190REAMER1 report
- RECLAIM 2976-20-240REAMER1 report
- RECLAIM 2976-21-140REAMER1 report
- RECLAIM 2976-21-190REAMER1 report
- RECLAIM 2976-23-240REAMER1 report
- RECLAIM 2976-25-240REAMER1 report
- RECLAIM 10-285-4518Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-285-4520Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4523Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4524Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4014Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4015Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4017Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4018Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4514Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4515Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 10-235-4517Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 34-185-0017REAMER1 report
- RECLAIM 34-185-0013REAMER1 report
- RECLAIM 34-235-0018REAMER1 report
- RECLAIM 44-00000-41SCREWDRIVER1 report
- RECLAIM 54-00000-01TRAY, SURGICAL, INSTRUMENT1 report
- RECLAIM 54-00000-05TRAY, SURGICAL, INSTRUMENT1 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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