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
- 11,618
- Deaths
- 45
- Injuries
- 9,863
- Malfunctions
- 1,710
Reports per year
110
513
714
715
516
717
50718
2,31719
2,19120
1,64721
1,27122
78523
61424
1,30725
94726
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Mesh, Surgical, PolymericFTL9,876
- Staple, ImplantableGDW817
- Laparoscope, General & Plastic SurgeryGCJ281
- Surgical FilmOOD221
- Mesh, Surgical, Absorbable, Abdominal HerniaOWT199
- Agent, Absorbable Hemostatic, Non-Collagen BasedLMG86
- Mesh, SurgicalFTM61
- Lavage, JetFQH22
- Agent, Absorbable Hemostatic, Collagen BasedLMF22
- Collagen Surgical Mesh Containing DrugsPIJ18
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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