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
- 1,949
- Deaths
- 57
- Injuries
- 718
- Malfunctions
- 1,174
Reports per year
123
1,94826
Source: FDA adverse event reports by year received, 2023–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT946
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS444
- Catheter, IrrigationGBX132
- Set, Administration, IntravascularFPA112
- Catheter, Hemodialysis, ImplantedMSD66
- System, Imaging, Pulsed Echo, UltrasonicIYO53
- Transducer, Ultrasonic, DiagnosticITX45
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ38
- Introducer, CatheterDYB31
- Needle, Hypodermic, Single LumenFMI19
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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