BD Nexiva 383571Recalls & reported problems
Becton, Dickinson And Company · NEXIVA 24GA X 0.75IN DP WITH MAXZERO · Class 2
All models of BD Nexiva (25)
Data updated Oct 16, 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 00382903835713), received between May 14, 2021 and Aug 7, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Activation” (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 16, 2026.
Most reported problems
Device problems
- Difficult or Delayed Activation1
Patient problems
- Hemorrhage/Blood Loss/Bleeding1
- Laceration(s)1
- 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.
MalfunctionAug 7, 2023
NURSE WAS INSERTING IV INTO PEDIATRIC PATIENT AND DID NOT GET THE USUAL FLASH VERIFYING VEIN PLACEMENT. ONCE IV CANNULA REMOVED, NURSE NOTE BLOOD IN CATHETER AND HAD BEEN INSERTED IN VEIN. ALSO NOTED VEIN "BLEW" AFTER REMOVAL.
Patient problems: Hemorrhage/Blood Loss/Bleeding; Laceration(s)
MAUDE report 17469572 ↗MalfunctionMay 14, 2021Difficult or Delayed Activation; Difficult or Delayed Activation
IT WAS REPORTED WHEN USING THE BD NEXIVA¿ CLOSED IV CATHETER SYST., DUAL PORT, MAXZERO¿ NEEDLE-FREE CONNECTOR, THE DEVICE EXPERIENCED SAFETY MECHANISM, NEEDLE DISENGAGEMENT (REMOVAL) DIFFICULTY. THIS EVENT OCCURRED THREE TIMES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "STIFF CANNULA, DIFFICULT TO REMOVE DESPITE LOOSENING." FOLLOW UP "I'VE HAD A FEW PROBLEMS WITH REALLY STIFF CANNULAS AS I'VE TRIED WITHDRAWING THE NEEDLE AND AS A RESULT, I'VE 'BLOWN' A FEW VEIN'S ANNOYINGLY, VEIN'S I PREVIOUSLY WOULDN'T HAVE DONE THIS TO. THIS IS DESPITE LOOSENING THE DEVICE BEFORE USE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825595 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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