BD Eclipse™ Needle with SmartSlip™ Technology 305888Recalls & reported problems
Becton, Dickinson And Company · NEEDLE ECLIPSE S/T 20X1-1/2 RB · Class 2
All models of BD Eclipse Needle with SmartSlip Technology (8)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382903058884), received between Jan 31, 2021 and Jan 31, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Leak/Splash” (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.
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- Exposure to Body Fluids1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 31, 2021Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE EXPERIENCED BLOOD EXPOSURE/SPLASH. IT HAS NOT BEEN SPECIFIED WHETHER MEDICAL INTERVENTION WAS APPLIED AS A RESULT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE CLIENT INFORMS US THAT A NURSE HAS HAD AN ACCIDENT EXPOSURE TO BLOOD WITH THE FOLLOWING PRODUCT: BD ECLIPSE REF 305888, LOT 1805008.
Patient problems: Exposure to Body Fluids
MAUDE report 11256406 ↗
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
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- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 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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