Howmedica Inc.
FDA adverse event reports naming Howmedica Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HOWMEDICA INC..
- Total reports
- 2,651
- Deaths
- 31
- Injuries
- 948
- Malfunctions
- 1,667
Reports per year
594
495
18096
74597
1,01598
46099
17100
6701
402
Source: FDA adverse event reports by year received, 1994–2002. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH645
- Orthopedic Manual Surgical InstrumentLXH319
- Bone CementLOD262
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB196
- Prosthesis, Knee, Hemi-, Patellar Resurfacing, UncementedHTG123
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH117
- ScrewdriverHXX85
- Rod, Fixation, Intramedullary And AccessoriesHSB80
- Screw, Fixation, BoneHWC80
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT76
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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