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
- 10,845
- Deaths
- 44
- Injuries
- 9,091
- Malfunctions
- 1,710
Reports per year
112
513
714
715
516
717
45518
2,08119
2,13920
1,54521
1,06022
67223
60624
1,30725
94726
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Mesh, Surgical, PolymericFTL9,112
- Staple, ImplantableGDW817
- Laparoscope, General & Plastic SurgeryGCJ281
- Surgical FilmOOD220
- Mesh, Surgical, Absorbable, Abdominal HerniaOWT192
- Agent, Absorbable Hemostatic, Non-Collagen BasedLMG86
- Mesh, SurgicalFTM60
- 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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