Davol Inc., SUB. C.R. Bard, Inc.
FDA adverse event reports naming Davol Inc., SUB. C.R. Bard, Inc. 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..
- Total reports
- 56,618
- Deaths
- 379
- Injuries
- 54,784
- Malfunctions
- 1,247
Reports per year
55712
63513
44014
42715
58616
1,13217
4,44018
10,28219
9,38720
8,28221
6,91922
5,05023
4,87724
16625
126
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, PolymericFTL54,441
- Staple, ImplantableGDW698
- Surgical FilmOOD485
- Mesh, Surgical, Absorbable, Abdominal HerniaOWT302
- Mesh, SurgicalFTM248
- Laparoscope, General & Plastic SurgeryGCJ118
- Lavage, JetFQH91
- Collagen Surgical Mesh Containing DrugsPIJ62
- Agent, Absorbable Hemostatic, Non-Collagen BasedLMG43
- Sealant, PolymerizingNBE29
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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