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
- 4,878
- Deaths
- 7
- Injuries
- 3,110
- Malfunctions
- 1,761
Reports per year
2412
4613
11214
38115
11516
22217
85218
1,01319
1,11020
48621
16322
10923
13124
4225
5226
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, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA1,530
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD604
- BroachHTQ445
- Orthopedic Manual Surgical InstrumentLXH411
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO387
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS360
- ScrewdriverHXX349
- Shoulder Prosthesis, Reverse ConfigurationPHX108
- Prosthesis, Hip, Hemi-, Femoral, MetalKWL104
- ImpactorHWA53
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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