Becton Dickinson Medical (singapore)
FDA adverse event reports naming Becton Dickinson Medical (singapore) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON MEDICAL (SINGAPORE).
- Total reports
- 5,368
- Deaths
- 4
- Injuries
- 421
- Malfunctions
- 4,942
Reports per year
104
2115
9316
26017
48918
98119
92620
98121
82122
61923
11624
1425
4626
Source: FDA adverse event reports by year received, 2004–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ2,754
- Needle, Hypodermic, Single LumenFMI1,289
- Syringe, PistonFMF947
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA266
- Set, Administration, IntravascularFPA42
- Accessories, Implant, Dental, EndosseousNDP27
- Wire, Guide, CatheterDQX12
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS6
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDWF5
- Needle, Aspiration And Injection, DisposableGAA3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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