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
- 6,921
- Deaths
- 3
- Injuries
- 2,495
- Malfunctions
- 564
Reports per year
64712
70013
84114
79315
46816
20917
618
13719
320
5021
3422
623
124
11325
226
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS2,113
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,360
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH622
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH327
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA270
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY229
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD210
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI202
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO201
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + AdditiveOIY192
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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