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
- 3,340
- Deaths
- 0
- Injuries
- 3,298
- Malfunctions
- 42
Reports per year
4117
218
1019
7420
41021
34222
1,42923
84724
18526
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Shoulder Prosthesis, Reverse ConfigurationPHX719
- 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.
Monitor Encore Medical L.P 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.