BD Nexiva™ Closed IV Catheter System 383646Recalls & reported problems
Becton, Dickinson And Company · BD Nexiva™ Closed IV Catheter System 20GA x 1.00IN · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903836468), received between Jan 10, 2025 and Jan 27, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions2
- Air Embolism1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 27, 2026Fluid/Blood Leak
IT WAS REPORTED THAT BD NEXIVA 20GA 1.00IN HF Y W/ CAP LEAKED AT CATHETER JUNCTION BLOOD LEAKAGE WITHIN CATHETER HUB WHEN DID THE INCIDENT OCCUR? DURING USE IT WAS REPORTED THAT THE IV G20 WAS NOT WORKING PROPERLY, WHEN THE IV INSERTED IMEDIATELY IT WAS LEAKING BLOOD FROM THE GRAY PART.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24189513 ↗MalfunctionJan 27, 2026Fluid/Blood Leak
IT WAS REPORTED THAT BD NEXIVA 20GA 1.00IN HF Y W/ CAP LEAKED AT CATHETER JUNCTION BLOOD LEAKAGE WITHIN CATHETER HUB WHEN DID THE INCIDENT OCCUR? DURING USE IT WAS REPORTED THAT THE IV G20 WAS NOT WORKING PROPERLY, WHEN THE IV INSERTED IMEDIATELY IT WAS LEAKING BLOOD FROM THE GRAY PART.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24189512 ↗InjuryJan 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT BD NEXIVA HF Y W/CAP AIR EMBOLISM REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: AIR EMBOLISM DURING CT SCAN WHILE USING BD NEXIVA. AIR COLUMN WAS NOTICED DURING THE SCAN REVIEW 21-DEC-2024 - RECEIVED AN EMAIL RESPONSE FROM COMPLAINANT FOR INFORMATION REQUESTED. 1.PROVIDE THE EVENT OCCURRENCE DATE. ANS: 19/12 2. PROVIDE THE LOT NUMBER ANS: UNKNOWN. CANNULA WAS SET IN THE GENERAL WARD AND WENT DOWN TO RADIOLOGY FOR A SCAN WHERE THE ISSUE OCCUR CUSTOMER RESPONSE (B)(6) 2025 WAS AIR NOTED IN THE NEXIVA TUBING? ANS : NO , DO TAKE NOTE THAT PATIENT WAS UNDERGOING CT SCAN , HIGH FLOW. WAS AIR NOTED IN THE IV TUBING? ANS : NO , DO TAKE NOTE THAT PATIENT WAS UNDERGOING CT SCAN , HIGH FLOW. WAS THERE ANY DAMAGE EVIDENT TO THE NEXIVA? ANS : NO , BUT Q-SYTE WAS NOT REPLACED DURING POWER INJECTION . HAVE ALREADY INFORMED THE HOSPITAL ON THE NEED TO REMOVE Q-SYTE BEFORE POWER INJECTION.
Patient problems: Air Embolism
MAUDE report 21131438 ↗
Other Catheter, intravascular, therapeutic, short-term less than 30 days devices
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- BD Insyte Autoguard 382533Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls527 reports
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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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