BD Eclipse 305769Recalls & reported problems
Becton, Dickinson And Company · NEEDLE ECLIPSE 23X1-1/4 RB · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903057696), received between Jul 15, 2019 and Oct 11, 2022 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Material Protrusion/Extrusion” (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.
Most reported problems
Device problems
- Material Protrusion/Extrusion2
- Detachment of Device or Device Component1
- Device Contamination with Chemical or Other Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Needle Stick/Puncture1
- No Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 11, 2022Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BLACK FOREIGN MATTER WAS FOUND IN THE CAP OF THE BD ECLIPSE¿ NEEDLE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE: "THERE IS A BLACK FOREIGN MATTER IN THE CAP OF THE SAFETY NEEDLE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15580948 ↗MalfunctionNov 15, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED WHEN USING THE BD ECLIPSE¿ NEEDLE 23X1-1/4 RB THE SAFETY MECHANISM DETACHES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: THE "PINK SHIELD DISCONNECTED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12816359 ↗InjuryFeb 16, 2021Material Protrusion/Extrusion
IT WAS REPORTED THAT NEEDLE ECLIPSE 23X1-1/4 RB HAD A SAFETY MECHANISM FAILURE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: SAFETY DIDNT ENGAGE PROPERLY. NEEDLESTICK INJURY CAUSED BY THE SAFETY NOT ENGAGING PROPERLY.
Patient problems: Needle Stick/Puncture; No Information
MAUDE report 11336184 ↗MalfunctionJul 15, 2019Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED THAT THE SAFETY MECHANISM LOOSENED AFTER USE WHILE RETRACTING THE BD ECLIPSE¿ NEEDLE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM (B)(6) TO ENGLISH: "IT'S NOTICED THAT SAFETY MECHANISM ON THE ECLIPSE NEEDLE LOOSEN AFTER NEEDLE RETRACTION"
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8791426 ↗
Other Needle, hypodermic, single lumen devices
- BD Nano 2nd Gen 320550Becton Dickinson Pen Limited · Needle, hypodermic, single lumen2,044 reports
- BD SafetyGlide 305916Becton, Dickinson And Company · Needle, hypodermic, single lumen1,767 reports
- BD Nano Ultra-Fine 320122Becton Dickinson Pen Limited · Needle, hypodermic, single lumen601 reports
- 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
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.