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
- 6,791
- Deaths
- 4
- Injuries
- 216
- Malfunctions
- 6,571
Reports per year
615
1716
35417
77318
1,02719
1,16320
1,30821
78722
78523
18925
38226
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
- Syringe, PistonFMF2,427
- Needle, Hypodermic, Single LumenFMI2,072
- Saline, Vascular Access FlushNGT1,450
- Needle, Aspiration And Injection, DisposableGAA573
- 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.
Monitor BD Medical (BD West) Medical Surgical automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.