BD Eclipse™ Needle with SmartSlip™ Technology 302436Recalls & reported problems
Becton, Dickinson And Company · NEEDLE 27X1-1/2 ECLIPSE · 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
- 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 00382903024360), received between Jun 4, 2019 and Jun 4, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Markings/Labelling 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.
Most reported problems
Device problems
- Device Markings/Labelling Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 4, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT NEEDLE 27X1-1/2 ECLIPSE CAME WITH A MIX OF PRODUCT TYPES IN A PACK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WE HAVE DELIVERED BD ECLIPSE NEEDLES 0.4MMX40MM TO THE CLIENT. A WEEK LATER THE CLIENT RETURNED THAT THERE WERE ALSO 'SHORT' NEEDLES BETWEEN THE NEEDLES, WHICH TURNED OUT TO BE 0.4MMX13MM NEEDLES. AT FIRST I THOUGHT THAT WE HAD FILLED OUT THE WRONG PART OF THE NEEDLES OURSELVES (TAKEN PART OF THE WRONG BOX), BUT IT TURNED OUT THAT WE DIDN'T HAVE THE NEEDLES OF 0.4MM X 13MM AND THAT WE DIDN'T HAVE ANY NEEDLES AFTER RESEARCH (AFTER CHECKING THE STOCK AND WHOLESALE DATA). IT SEEMS THAT IN THE BOX OF 0,4X40MM THERE WERE WRONG NEEDLES OF 0,4X13 MM. THIS IS THE CASE: BD ECLIPSE NEEDLE 0.4X40 MM REF 302436, LOT NO 1808001, VVD 2023-07 AND THE NEEDLES FOUND ARE: BD ECLIPSE NEEDLE 0.4MMX13MM REF 305770, VVD 2022-11, VVD 1712001.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8666990 ↗
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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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