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
- 1,367
- Deaths
- 27
- Injuries
- 615
- Malfunctions
- 719
Reports per year
1201
1002
103
12904
15705
25506
26207
10608
5809
4910
6211
6212
6713
13614
115
Source: FDA adverse event reports by year received, 2001–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS496
- Tubes, Gastrointestinal (And Accessories)KNT361
- Catheter, Intravascular, DiagnosticDQO181
- Catheter, Hemodialysis, ImplantedMSD143
- Catheter, SubclavianLFJ50
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ28
- Introducer, CatheterDYB21
- Set, Administration, IntravascularFPA21
- Catheter, Hemodialysis, Non-ImplantedMPB21
- Tube, Gastro-EnterostomyKGC13
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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