Davol Inc., Sub. C.R. Bard, Inc. -1213643
FDA adverse event reports naming Davol Inc., Sub. C.R. Bard, Inc. -1213643 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: Davol Inc., Sub. C.R. Bard, Inc. -1213643.
- Total reports
- 1,407
- Deaths
- 9
- Injuries
- 1,371
- Malfunctions
- 27
Reports per year
108
109
110
112
5218
25819
28420
21521
18022
9523
2524
29426
Source: FDA adverse event reports by year received, 2008–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Mesh, Surgical, PolymericFTL1,324
- Mesh, Surgical, Absorbable, Abdominal HerniaOWT27
- Surgical FilmOOD23
- Staple, ImplantableGDW17
- Mesh, SurgicalFTM9
- Agent, Absorbable Hemostatic, Non-Collagen BasedLMG3
- Collagen Surgical Mesh Containing DrugsPIJ2
- Tray, Surgical, InstrumentFSM1
- Agent, Absorbable Hemostatic, Collagen BasedLMF1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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