BD Nexiva™ Closed IV Catheter System 383649Recalls & reported problems
Becton, Dickinson And Company · BD Nexiva™ Closed IV Catheter System 18GA x 1.25IN · Class 2
All models of BD Nexiva Closed IV Catheter System (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903836499), received between Jan 5, 2024 and May 11, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Separation” (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.
Reports received per month
Most reported problems
Device problems
- Difficult or Delayed Separation1
- Fluid/Blood Leak1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 11, 2026Material Integrity Problem
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25137721 ↗MalfunctionApr 1, 2024Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT BD NEXIVA LEAKED AT THE SEPTUM. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: IF LEAKAGE FROM THE ISOLATION PLUG IS FOUND DURING PRODUCT USE, A COMPLAINT REPLY LETTER, A COMPLAINT ACCEPTANCE LETTER, AND A GREEN CLAIM ARE REQUIRED. THE SAMPLE CANNOT BE RETURNED. A VIDEO IS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19015152 ↗MalfunctionJan 5, 2024Difficult or Delayed Separation; Difficult or Delayed Separation
IT WAS REPORTED THAT BD INEXIVA 24GA 0.75IN Y WAS DIFFICULT TO WITHDRAW. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: PATIENT FOUND UNABLE TO WITHDRAW THE NEEDLE CORE DURING USE, NEED TO USE TWEEZERS TO TWIST THE TIP PROTECTOR LOOSE BEFORE WITHDRAWING, PATIENT BLEEDING HEAVILY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18454183 ↗
Other Catheter, intravascular, therapeutic, short-term less than 30 days devices
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- BD Insyte Autoguard Shielded IV Catheter 381823Becton, Dickinson And Company · Catheter, intravascular, therapeutic, short-term less than 30 days582 reports
- BD Insyte Autoguard 381423Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall528 reports
- BD Insyte Autoguard 382544Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall437 reports
- 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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