BD Nexiva 383545Recalls & reported problems
Becton, Dickinson And Company · NEXIVA 18GA 1.25IN DP WITH NO CONNECTOR · Class 2
All models of BD Nexiva (25)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903835454), received between Feb 27, 2020 and Aug 16, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Leak/Splash2
- Device Contamination with Chemical or Other Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 16, 2022Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD NEXIVA¿ 18GA 1.25IN DP WITH NO CONNECTOR LEAKED FROM THE PLUG. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN THE NEEDLE PART WAS REMOVED, THE GREY RUBBER PLUG FAILED TO SEAL THE END OF THE IV BUTTERFLY/FLANGE AND BLOOD FREELY FLOWED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15234488 ↗MalfunctionFeb 27, 2020Leak/Splash; Device Contamination with Chemical or Other Material; Leak/Splash; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT LEAKAGE OCCURRED DURING USE WITH A BD NEXIVA¿ CLOSED IV CATHETER SYSTEM - DUAL PORT 18 GA 1.25 IN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, "THIS MORNING WE HAVE HAD A FAILURE OF A NUMBER 18 IV CANNULA. INSERTED WELL, BUT STARTED SPEWING BLOOD FROM THE CATHETER RIGHT CLOSE TO THE WINGS. WHEN LOOKED CLOSELY AT THE CATHELON, WE SAW BLOOD SPEWING FROM A HOLE IN THE CATHETER."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9766040 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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