BD Eclipse™ Needle with SmartSlip™ Technology 305899Recalls & reported problems
Becton, Dickinson And Company · NEEDLE ECLIPSE S/T 20X1 RB · 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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903058990), received between Nov 26, 2020 and Dec 29, 2020 — classified as 2 malfunctions.
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 16, 2026.
Most reported problems
Device problems
- Leak/Splash1
- Material Protrusion/Extrusion1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 29, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE NEEDLE ECLIPSE S/T 20X1 RB SEPARATED FROM THE SYRINGE DURING AN INTRAMUSCULAR INJECTION OF "HALDOL DECANOAS". THIS COMPLAINT WAS CREATED TO CAPTURE THE 4TH OF 4 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM FRENCH TO ENGLISH: "OUR PROBLEM OCCURS WHEN INJECTING HALDOL DECANOAS (OILY PRODUCT): THE NEEDLE COMES LOOSE FROM THE SYRINGE. IT IS LIKELY THAT THIS HAPPENS BECAUSE THE NEEDLE IS NOT HELD IN PLACE WHEN THE PLUNGER OF THE SYRINGE IS PRESSED." "THIS PROBLEM FREQUENTLY OCCURS WHEN PERFORMING AN INTRAMUSCULAR (IM) INJECTION AND EVEN MORE SO IF THE PRODUCT IS OILY AND/OR VISCOUS. OVERPRESSURE CAUSES THE NEEDLE AND SYRINGE TO DISSOCIATE. AND FOR HAVING PRACTICED THIS TYPE OF INJECTION IT HAPPENS WITH ANY IM. SO I DON'T THINK THIS IS RELATED TO BD DMS IN PARTICULAR." "ANOTHER FACTOR PROMOTING DISSOCIATION IS THE USE OF LUER SLIP SYRINGES RATHER THAN LUER LOCK."
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11089402 ↗MalfunctionNov 26, 2020Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED THAT A NEEDLE ECLIPSE S/T 20X1 RB HAD A BROKEN SAFETY MECHANISM DURING USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "TODAY, AFTER ADMINISTERING THE FLU SHOT TO A COLLEAGUE, THE CAP BROKE OFF WHEN "CLICKING" THE CAP OVER THE NEEDLE. THIS HAPPENED VERY SUDDENLY SO I ALMOST PRICKED MYSELF TO THE USED NEEDLE. I THINK IT IS IMPORTANT FOR YOU TO KNOW.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10909602 ↗
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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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