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
- 3,343
- Deaths
- 0
- Injuries
- 3,301
- Malfunctions
- 42
Reports per year
4117
218
1019
7420
41021
34222
1,42923
84724
18826
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Shoulder Prosthesis, Reverse ConfigurationPHX721
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS672
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH459
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH343
- Guide, Surgical, InstrumentFZX309
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO248
- Prosthesis, Elbow, Constrained, CementedJDC133
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, CementedPAO69
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH56
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + AdditiveOIY56
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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