BD Medical (BD West) Medical Surgical
FDA adverse event reports naming BD Medical (BD West) Medical Surgical as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BD MEDICAL (BD WEST) MEDICAL SURGICAL.
- Total reports
- 6,826
- Deaths
- 4
- Injuries
- 222
- Malfunctions
- 6,600
Reports per year
615
1716
35417
77318
1,02719
1,16320
1,30821
78722
78523
18925
41726
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
- Syringe, PistonFMF2,437
- Needle, Hypodermic, Single LumenFMI2,081
- Saline, Vascular Access FlushNGT1,453
- Needle, Aspiration And Injection, DisposableGAA586
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ93
- Syringe, Irrigating (Non Dental)KYZ57
- Heparin, Vascular Access FlushNZW35
- Syringe, AntistickMEG33
- Set, Administration, IntravascularFPA18
- Tubes, Gastrointestinal (And Accessories)KNT15
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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