BD (suzhou)
FDA adverse event reports naming BD (suzhou) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BD (SUZHOU).
- Total reports
- 3,776
- Deaths
- 0
- Injuries
- 267
- Malfunctions
- 3,509
Reports per year
815
3516
18217
37518
84119
65320
42921
36522
74523
11724
2525
126
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, Short-Term Less Than 30 DaysFOZ3,001
- Needle, Hypodermic, Single LumenFMI299
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA235
- Set, Administration, IntravascularFPA148
- Anesthesia Conduction KitCAZ34
- Syringe, PistonFMF23
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS10
- Midline CatheterPND8
- Set, I.V. Fluid TransferLHI4
- Blood/Plasma Collection Device For Dna TestingPJE3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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