BD Suzhou (mds)
FDA adverse event reports naming BD Suzhou (mds) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BD SUZHOU (MDS).
- Total reports
- 1,674
- Deaths
- 0
- Injuries
- 42
- Malfunctions
- 1,632
Reports per year
79524
53825
34126
Source: FDA adverse event reports by year received, 2024–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ1,598
- Stopcock, I.V. SetFMG34
- Set, Administration, IntravascularFPA33
- Syringe, PistonFMF5
- Needle, Hypodermic, Single LumenFMI1
- Needle, Aspiration And Injection, DisposableGAA1
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS1
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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