Stryker Orthopaedics Limerick
FDA adverse event reports naming Stryker Orthopaedics Limerick as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER ORTHOPAEDICS LIMERICK.
- Total reports
- 1,952
- Deaths
- 47
- Injuries
- 1,046
- Malfunctions
- 783
Reports per year
3404
6405
6706
6307
10708
25909
52010
45311
37612
913
Source: FDA adverse event reports by year received, 2004–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH744
- Bone CementLOD496
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH144
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH105
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO83
- Methyl Methacrylate For CranioplastyGXP73
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI67
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerHSX36
- Orthopedic Manual Surgical InstrumentLXH35
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY34
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Stryker Orthopaedics Limerick automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.