C. R. Bard Inc. (basd)
FDA adverse event reports naming C. R. Bard Inc. (basd) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: C. R. BARD INC. (BASD).
- Total reports
- 1,605
- Deaths
- 37
- Injuries
- 563
- Malfunctions
- 995
Reports per year
21808
27109
24010
23811
27212
36613
Source: FDA adverse event reports by year received, 2008–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS849
- Tubes, Gastrointestinal (And Accessories)KNT263
- Catheter, Hemodialysis, ImplantedMSD258
- Set, Administration, IntravascularFPA63
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ42
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT31
- Catheter, Hemodialysis, Non-ImplantedMPB25
- Catheter, SubclavianLFJ18
- Catheter, Intravascular, DiagnosticDQO10
- Introducer, CatheterDYB10
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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