Depuy Orthopaedics Inc US
FDA adverse event reports naming Depuy Orthopaedics Inc US as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DePuy Orthopaedics Inc US.
- Total reports
- 2,319
- Deaths
- 0
- Injuries
- 1,378
- Malfunctions
- 941
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH484
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH248
- ImpactorHWA174
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO151
- Orthopedic Manual Surgical InstrumentLXH148
- Bit, DrillHTW130
- TemplateHWT116
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI115
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD94
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL81
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Depuy Orthopaedics Inc US automatically
DeviceWatch monitors available FDA adverse events and recalls. Growth includes event alerts for Death and Injury reports; Compliance Pro adds safety signals for investigation. FDA publication delays and incomplete collection or analysis coverage limit detection; no signal does not establish the absence of a safety concern. AI summaries and signals are provisional and require human review.