Encore Medical L.P.
FDA adverse event reports naming Encore Medical L.P. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ENCORE MEDICAL L.P..
- Total reports
- 10,624
- Deaths
- 1
- Injuries
- 10,402
- Malfunctions
- 199
Reports per year
2610
111
114
215
616
76017
86018
1,10919
1,08320
87221
1,40722
43923
1,21524
1,98825
83326
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS2,183
- Shoulder Prosthesis, Reverse ConfigurationPHX2,175
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,965
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH1,016
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO809
- Prosthesis, Elbow, Constrained, CementedJDC527
- Guide, Surgical, InstrumentFZX316
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + AdditiveOIY210
- Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, UncementedOQG189
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH155
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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