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
- 11,409
- Deaths
- 48
- Injuries
- 9,658
- Malfunctions
- 1,703
Reports per year
112
513
714
715
516
717
53818
2,36219
2,29620
1,53321
1,16822
71023
61224
1,30725
85026
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
- Mesh, Surgical, PolymericFTL9,683
- Staple, ImplantableGDW811
- Laparoscope, General & Plastic SurgeryGCJ281
- Surgical FilmOOD221
- Mesh, Surgical, Absorbable, Abdominal HerniaOWT191
- Agent, Absorbable Hemostatic, Non-Collagen BasedLMG85
- 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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