LPSRecalls & reported problems across all models
Depuy (Ireland) · 113 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
LPS models — page 2
113 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- LPS 2987-14-111TEMPLATE1 report
- LPS 2987-22-116TEMPLATE1 report
- LPS 2987-22-212TEMPLATE1 report
- LPS 2987-22-214TEMPLATE1 report
- LPS 2987-22-216TEMPLATE1 report
- LPS 2987-22-218TEMPLATE1 report
- LPS 2987-22-221TEMPLATE1 report
- LPS 2987-22-314TEMPLATE1 report
- LPS 2987-22-321TEMPLATE1 report
- LPS 2987-70-110REAMER1 report
- LPS 2987-70-130REAMER1 report
- LPS 2987-72-040HAMMER, SURGICAL1 report
- LPS 2987-99-032TRAY, 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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