Becton Dickinson Medical Systems
FDA adverse event reports naming Becton Dickinson Medical Systems as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON MEDICAL SYSTEMS.
- Total reports
- 9,811
- Deaths
- 22
- Injuries
- 361
- Malfunctions
- 9,425
Reports per year
Source: FDA adverse event reports by year received, 2006–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Syringe, PistonFMF6,086
- Needle, Hypodermic, Single LumenFMI2,743
- Syringe, AntistickMEG639
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ131
- Container, Liquid Medication, GraduatedKYW129
- Set, Administration, IntravascularFPA23
- Piston Syringe With Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact QEH18
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA17
- Tubes, Gastrointestinal (And Accessories)KNT14
- Saline, Vascular Access FlushNGT3
Recent recalls
- 2010-02-02TerminatedProcess control
BD Q-Syte, Luer Access Split-Septum, 0.10 ml, REF 385100, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
BD Q-Syte Extension Set, 15cm Std Bore, P.V. 1.14 ml Luer-Lok, REF 385101, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
BD Q-Syte Extension Set, 15 cm, P.V. 0.21 ml, REF 385102, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
BD Q-Syte Vial Access Adapter, 0.16 ml, REF 385108, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
MPS Acacia Extension Set, 15cm RightBore-18, Spin Nut w/BBD Q-Syte, REF 385150,
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
MPS Acacia Extension Set, 15cm Small Bore, Spin Nut w/BD Q-Syte, REF 385151
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
MPS Acacia Tri-Extension Set, 15cm Small Bore, Spin Nut w/BD Q-Syte, REF 385164
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
BD Nexiva Closed IV Catheter System, REF 383530, 24GA 0.56IN, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
BD Nexiva Closed IV Catheter System, REF 383531, 24GA 0.75IN, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
- 2010-02-02TerminatedProcess control
BD Nexiva Closed IV Catheter System, REF 383532, 22GA 1.00IN, Becton Dickinson Infusion Therapy Systems Inc.
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
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