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
- 42,407
- Deaths
- 297
- Injuries
- 9,519
- Malfunctions
- 32,591
Reports per year
1015
1,07420
5,26221
6,14222
6,10623
8,17024
10,67825
4,96526
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS16,404
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT10,877
- Set, Administration, IntravascularFPA3,335
- System, Imaging, Pulsed Echo, UltrasonicIYO2,470
- Catheter, IrrigationGBX2,445
- Catheter, Hemodialysis, ImplantedMSD1,990
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ1,246
- Introducer, CatheterDYB817
- Midline CatheterPND578
- Device, Intravascular Catheter SecurementKMK367
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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