BD Medical - Diabetes Care
FDA adverse event reports naming BD Medical - Diabetes Care as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BD MEDICAL - DIABETES CARE.
- Total reports
- 8,115
- Deaths
- 1
- Injuries
- 290
- Malfunctions
- 7,823
Reports per year
105
107
110
212
1015
6116
39217
97618
1,44519
1,83120
1,36421
96822
87723
17824
825
Source: FDA adverse event reports by year received, 2005–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Syringe, PistonFMF7,278
- Needle, Hypodermic, Single LumenFMI423
- Syringe, AntistickMEG286
- Pad, Alcohol, Device DisinfectantLKB91
- Set, Administration, IntravascularFPA16
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA12
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ3
- Tubing, Fluid DeliveryFPK1
- Needle, Aspiration And Injection, DisposableGAA1
- Culture Media, Non-Propagating TransportJSM1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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