BD Eclipse™ Needle with SmartSlip™ Technology 305894Recalls & reported problems
Becton, Dickinson And Company · NEEDLE ECLIPSE S/T 21X1 RB TW · Class 2
All models of BD Eclipse Needle with SmartSlip Technology (8)
Data updated Oct 16, 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 00382903058945), received between Nov 15, 2017 and Feb 18, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Fail-Safe 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fail-Safe Problem1
- Leak/Splash1
- Material Integrity Problem1
Patient problems
- Needle Stick/Puncture1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2026Material Integrity Problem
IT WAS REPORTED THAT THE BD NEEDLE ECLIPSE S/T 21X1 RB TW NEEDLE HUB WAS CRACKED / DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN LOADING PROPOFOL WITH A GREEN BD ECLIPSE NEEDLE, BATCH 2505002, 0.8X 25MM, A GREEN PARTICLE COMES OFF AND REMAINS INSIDE THE SYRINGE. THE PARTICLE IS VISIBLE AND THE MEDICATION IS NOT USED. ATTACHED IS A PHOTO OF WHAT HAPPENED, WHERE YOU CAN SEE THE PARTICLE INDICATED BY THE CUSTOMER. WHEN DID THE INCIDENT OCCUR? BEFORE USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24376500 ↗MalfunctionJul 2, 2019Leak/Splash; Leak/Splash
IT WAS REPORTED THAT BD¿ NEEDLE ECLIPSE SMARTSLIP HUB IS PERFORATED AND ALLOWED BLOOD TO LEAK. THIS WAS DISCOVERED DURING USE. NO DATE/TIME OR PATIENT INFORMATION WAS GIVEN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE HUB OF THE NEEDLE IS PERFORATED AND THERE WERE A BLOOD LEAKAGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8755469 ↗InjuryNov 15, 2017Fail-Safe Problem
IT WAS REPORTED THAT WHILE A NURSE WAS TAKING A BLOOD SAMPLE, THE SAFETY COVER ON A BD ECLIPSE¿ NEEDLE FAILED TO ACTIVATE CAUSING A NEEDLE STICK TO THE NURSE¿S RIGHT FOREFINGER. ANTIVIRALS WERE PRESCRIBED BUT COULD NOT BE TAKEN DUE TO CONTRAINDICATIONS WITH OTHER MEDICATIONS. COMPARATIVE BLOOD SAMPLES ARE SCHEDULED TO BE TAKEN OVER A THREE MONTH PERIOD. THERE WAS NO ADDITIONAL MEDICAL INFORMATION PROVIDED.
Patient problems: Needle Stick/Puncture
MAUDE report 7035800 ↗
Other Needle, hypodermic, single lumen devices
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- N/A 305106Becton, Dickinson And Company · Needle, hypodermic, single lumen1 recall467 reports
- N/A 305110Becton, Dickinson And Company · Needle, hypodermic, single lumen418 reports
- BD Safe-Clip 328235Becton, Dickinson and Company Inc · Needle, hypodermic, single lumen268 reports
- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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