BD Eclipse 305768Recalls & reported problems
Becton, Dickinson And Company · NEEDLE ECLIPSE 22X1 RB · Class 2
All models of BD Eclipse (12)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903057689), received between Apr 27, 2018 and Dec 10, 2020 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment Of Device Component” (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
- Detachment Of Device Component1
- Device Contamination with Body Fluid1
- Device Markings/Labelling Problem1
- Material Protrusion/Extrusion1
Patient problems
- No Known Impact Or Consequence To Patient2
- No Consequences Or Impact To Patient1
- No Patient Involvement1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 10, 2020Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED THAT THE NEEDLE ECLIPSE 22X1 RB EXPERIENCED A SAFETY MECHANISM THAT DETACHED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO:305768, BATCH NO: UNKNOWN. AFTER ADMINISTERING A FLU VACCINE, WHEN ATTEMPTING TO ENGAGE THE SAFETY CAP, IT POPPED OFF BD ECLIPSE NEEDLE 22G X 1.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10988673 ↗MalfunctionMar 25, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT 20 BD ECLIPSE¿ NEEDLES WERE FOUND AT "DOUBLE THE LENGTH THEY SHOULD BE" BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "DESCRIPTION: ITEM IS DESCRIBED AS 22G X 1" NEEDLE BUT THE NEEDLES ARE DOUBLE THE LENGTH THEY SHOULD BE. THEY HAVE ABOUT 20 OF THESE NEEDLES THEY FOUND DEFECTIVE".
Patient problems: No Patient Involvement
MAUDE report 9881123 ↗MalfunctionJan 28, 2019Device Contamination with Body Fluid
IT WAS REPORTED THAT TWENTY-TWO BD¿ ECLIPSE NEEDLES HAD DROPS OF BLOOD SPLATTER WHEN THE SAFETY DEVICES WERE ACTIVATED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8283735 ↗MalfunctionApr 27, 2018Detachment Of Device Component
IT WAS REPORTED THAT THE SAFETY MECHANISM ON A BD ECLIPSE¿ NEEDLE "FLEW OFF" WHEN ATTEMPTING TO ACTIVATE AFTER AN INJECTION. THERE WAS NO REPORT OF EXPOSURE, SERIOUS INJURY OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7470142 ↗
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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page