Zimmer TMT
FDA adverse event reports naming Zimmer TMT as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ZIMMER TMT.
- Total reports
- 1,328
- Deaths
- 0
- Injuries
- 1,166
- Malfunctions
- 156
Reports per year
15712
8013
8014
10515
8516
10617
7518
4419
10420
6721
2322
423
624
2525
4526
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, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH622
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH118
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH103
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI100
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS49
- Prosthesis, Shoulder, Non-Constrained, Metal/Polymer CementedKWT37
- Spinal Vertebral Body Replacement DeviceMQP35
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB33
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH31
- Orthopedic Manual Surgical InstrumentLXH25
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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