BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ 383598Recalls & reported problems
Becton, Dickinson And Company · NEXIVA DIFFUSICS w/MaxZero 22G X 1.75 IN · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382903835980), received between Jan 21, 2026 and Jan 21, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Retraction Problem” (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
- Retraction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 21, 2026Retraction Problem
IT WAS REPORTED THAT BD NEXIVA DIFFUSICS W/MAXZERO NEEDLE RETRACTION FAILED IT WAS REPORTED BY THE CUSTOMER THAT THE SAFETY MECHANISM DID NOT ACTIVATE. IT WAS STILL NESTED IN THE WHITE NEEDLE HOLDER AND THEY HAD TO PHYSICALLY PULL THE PLASTIC BOX DOWN TO THE NEEDLE TIP, AND IT STILL DIDN¿T CATCH, SO THEY PULLED IT DOWN WITH MORE FORCE AND IT HELD. RCC RECEIVED A COMPLAINT VIA EMAIL. I AM WRITING TO LET YOU KNOW OF A NEEDLE SAFETY MECHANISM FAILURE I EXPERIENCED THIS MORNING. I PLACED A 22G 1 ¾ IN. PIV THIS MORNING AND THE SAFETY MECHANISM DID NOT ACTIVATE. IT WAS STILL NESTED IN THE WHITE NEEDLE HOLDER AND I HAD TO PHYSICALLY PULL THE PLASTIC BOX DOWN TO THE NEEDLE TIP, AND IT STILL DIDN¿T CATCH, SO I PULLED IT DOWN WITH MORE FORCE AND IT HELD. THE CATHETER PACKAGING IS PICTURED BELOW. PLEASE LET ME KNOW IF YOU NEED ANYMORE INFORMATION. I HAVE SAVED THE NEEDLE IF YOU NEED IT. ITEM# 383598, LOT# 5247921.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24132921 ↗
Other Catheter, intravascular, therapeutic, short-term less than 30 days devices
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- BD Insyte Autoguard 381423Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall528 reports
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- 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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