Depuy France SAS 3003895575
FDA adverse event reports naming Depuy France SAS 3003895575 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY FRANCE SAS 3003895575.
- Total reports
- 2,821
- Deaths
- 5
- Injuries
- 2,072
- Malfunctions
- 744
Reports per year
110
611
1512
5513
28614
55215
44616
38617
49518
39019
920
5721
9622
2523
124
Source: FDA adverse event reports by year received, 2010–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA906
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD585
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS302
- Orthopedic Manual Surgical InstrumentLXH185
- BroachHTQ161
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO136
- ScrewdriverHXX131
- Prosthesis, Hip, Hemi-, Femoral, MetalKWL120
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY86
- Hammer, SurgicalFZY21
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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