BD Nexiva 383577Recalls & reported problems
Becton, Dickinson And Company · NEXIVA 20GA X 1.25 IN DP WITH MAXZERO · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903835775), received between Apr 29, 2021 and Sep 19, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (1 report).
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/Splash1
- Retraction Problem1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 19, 2022Retraction Problem; Retraction Problem
IT WAS REPORTED THAT THE BD NEXIVA¿ CLOSED IV CATHETER SYSTEM WITH BD MAXZERO¿ NEEDLE-FREE CONNECTOR NEEDLE WAS DIFFICULT TO REMOVE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 2ND OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "WHEN ADVANCING CATHETER, PLASTIC GUIDE GETTING SNAGGED WHEN TRYING TO ADVANCE PLASTIC CATHETER AND REMOVE NEEDLE FROM DEVICE... I HAVE HAD THIS HAPPEN WITH BOTH 20G AND 18G"
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15451742 ↗InjuryApr 29, 2021Leak/Splash; Leak/Splash
IT WAS REPORTED THAT NEXIVA 20GA X 1.25 IN DP WITH MAXZERO CATHETER DETACHED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO.: 383577, BATCH NO.: UNKNOWN. IT WAS REPORTED THAT NEEDLE DETACHED FROM HUB OF THE IV DAYS AFTER INSERTION. PER COMPLAINT DETAILS RECEIVED: NEXIVA CANNULA CAME DETACHED FROM HUB OF IV. THEY NOTICED DAYS AFTER INSERTION. THEY WERE NOT ABLE TO FIND THE CANNULA AFTER SCAN AND STUDIES.
Patient problems: Insufficient Information
MAUDE report 11748188 ↗
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- BD Nexiva, BD Q-Syte 383536Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls374 reports
- BD PosiFlush 306547Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls1 death331 reports
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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