C.R. Bard, Inc. (basd) -3006260740
FDA adverse event reports naming C.R. Bard, Inc. (basd) -3006260740 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: C.R. BARD, INC. (BASD) -3006260740.
- Total reports
- 42,958
- Deaths
- 308
- Injuries
- 9,713
- Malfunctions
- 32,937
Reports per year
1015
1,07420
5,26221
6,14222
6,10623
8,17024
10,67825
5,51626
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS16,580
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT11,082
- Set, Administration, IntravascularFPA3,365
- System, Imaging, Pulsed Echo, UltrasonicIYO2,483
- Catheter, IrrigationGBX2,480
- Catheter, Hemodialysis, ImplantedMSD2,006
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ1,263
- Introducer, CatheterDYB826
- Midline CatheterPND584
- Device, Intravascular Catheter SecurementKMK370
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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