Eclipse 305770Recalls & reported problems
Becton, Dickinson And Company · NEEDLE ECLIPSE S/T 27X1/2 RB · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903057702), received between Jul 25, 2025 and Sep 11, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem2
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 11, 2026Connection Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744356 ↗MalfunctionSep 11, 2026Connection Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50743251 ↗MalfunctionJul 25, 2025Break; Break
IT WAS REPORTED THAT BD NEEDLE ECLIPSE SAFETY SHIELD BROKE OFF. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE PROTECTIVE CAPS THAT ARE FOLDED OVER THE CANNULA AFTER USE FELL OFF AND THE CANNULAS HAD TO BE DISPOSED OF IN THE PUNCTURE-PROOF DISPOSAL BOXES WITHOUT ANY SAFETY PROTECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22613776 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.