BD Infusion Therapy Systems Inc. S.A. DE C.V.
FDA adverse event reports naming BD Infusion Therapy Systems Inc. S.A. DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V..
- Total reports
- 4,339
- Deaths
- 6
- Injuries
- 223
- Malfunctions
- 4,110
Reports per year
114
1515
6316
21017
46418
71919
46720
45321
54622
37323
39124
34125
29626
Source: FDA adverse event reports by year received, 2014–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ1,589
- Set, Administration, IntravascularFPA1,155
- Stopcock, I.V. SetFMG988
- Syringe, PistonFMF471
- Needle, Hypodermic, Single LumenFMI50
- Anesthesia Conduction KitCAZ20
- Device, Specimen CollectionLIO16
- Introducer, CatheterDYB14
- Dispenser, Liquid MedicationKYX11
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor BD Infusion Therapy Systems Inc. S.A. DE C.V. automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.