ExT™ Stabilized Extension Set with NearPort™ IV Access 390222Recalls & reported problems
Becton, Dickinson And Company · ExT Extension Set with Microclave NFC · Class 2
Data updated Oct 18, 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 00382903902224), received between Mar 18, 2024 and Jun 12, 2024 — classified as 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
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 12, 2024Fluid/Blood Leak; Fluid/Blood Leak
MATERIAL# 390222 BATCH# REHV2546 IT WAS REPORTED BY CUSTOMER THAT THE EXTENSION SET WAS LEAKING BLOOD AND HAD TO BE DISCONNECTED AND A NEW SET APPLIED. VERBATIM: EVN24543041 -- EXTENSION SET WAS LEAKING BLOOD SITUATION: ISSUE: IV WAS PLACED AND THE EXTENSION SET WAS LEAKING BLOOD AND HAD TO BE DISCONNECTED AND A NEW SET APPLIED. PT WAS ANXIOUS ABOUT IV AND IT COMPLICATED THE EXPERIENCE. REF 390222, LOT #REHV2546
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19521371 ↗MalfunctionMar 18, 2024Fluid/Blood Leak; Leak/Splash; Fluid/Blood Leak; Leak/Splash
IT WAS REPORTED THAT BD EXT EXTENSION SET WITH MICROCLAVE NFC LEAKED AT CONNECTION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE IV EXTENSION TUBING LEAKED FROM THE CONNECTION POINT WHERE THE EXTENSION TUBING ENTERS THE IV BASE/HUB, IV FLUID AND BLOOD SPILLED ON PATIENT AND BED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18922355 ↗
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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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