BD Luer-Lok, BD Eclipse 305783Recalls & reported problems
Becton, Dickinson And Company · SYRINGE 3ML LL W/NDL ECLIPSE 22X1-1/2 RB · Class 2
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 00382903057832), received between Oct 25, 2017 and Aug 9, 2024 — classified as 1 injury, 11 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (4 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
- Leak/Splash4
- Break2
- Fluid/Blood Leak2
- Bent1
- Device Contamination with Chemical or Other Material1
- Device Markings/Labelling Problem1
- Material Protrusion/Extrusion1
Patient problems
- No Known Impact Or Consequence To Patient9
- Foreign Body In Patient1
- No Information1
- No Patient Involvement1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
InjuryAug 9, 2024Break; Break
IT WAS REPORTED THAT BD SYRINGE 3ML LL W/NDL ECLIPSE 22X1-1/2 RB NEEDLE BROKE. IT WAS REPORTED BY CUSTOMER THAT THE PATIENT RETURNED AFTER 15 DAYS OF AN INJECTION COMPLAINING OF SWELLING AND PAIN AT INJECTION SITE, UPON EXAMINATION A TINY PIECE OF NEEDLE TIP WAS FOUND IN THE SITE. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. GAVE B12 INJECTION IM, PATIENT RETURNED 15 DAYS LATER WITH SWELLING AND PAIN AT INJECTION SITE, UPON EXAMINATION PHYSICIAN FOUND A TINY NEEDLE TIP IN THE SITE.
Patient problems: Foreign Body In Patient
MAUDE report 19951283 ↗MalfunctionNov 25, 2019Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED THAT BD ECLIPSE¿ 3 ML BD LUER-LOK¿ SYRINGE SAFETY MECHANISM DETACHED. THIS WAS DISCOVERED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305783, BATCH NO: 9081645. IT WAS REPORTED THAT WHEN NURSE ATTEMPTED TO ACTIVATE SAFETY MECHANISM, THE ARM DISENGAGED FROM THE HINGES AND FELL OFF. NURSE ATTEMPTED TO ACTIVATE THE SAFETY MECHANISM AND THE ARM DISENGAGED FROM THE HINGES AND FELL OFF.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9369906 ↗MalfunctionAug 13, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem
MATERIAL NO. 305783, BATCH NO. 8333678. IT WAS REPORTED THAT DURING USE OF THE BD ECLIPSE¿ BD LUER-LOK¿ SYRINGE WITH NEEDLE THE PACKAGES WAS LABELED AS 3M 22G X 1.5 NEEDLE BUT CONTAINED ONE INCH NEEDLES IN THE PACKAGE. 25 SYRINGES WERE FOUND TO BE LABELED THIS WAY. FOUND 25 SYRINGES ON THE SHELF THAT ARE LABELLED 3M 22G X 1.5 NEEDLE THAT IN HAVE 1 I" NEEDLES IN THE PACKAGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8890873 ↗MalfunctionFeb 27, 2019Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BEFORE USE OF THE BD ECLIPSE¿ BD LUER-LOK¿ SYRINGE WITH NEEDLE THE SYRINGE WAS DISCOLORED AND APPEARED DIRTY.
Patient problems: No Information
MAUDE report 8375493 ↗MalfunctionJan 8, 2019Break
IT WAS REPORTED THAT BD ECLIPSE¿ BD LUER-LOK¿ SYRINGE WITH NEEDLE SAFETY CLIP BROKE OFF. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8227888 ↗MalfunctionJul 17, 2018Fluid/Blood Leak
IT WAS REPORTED THAT BD ECLIPSE¿ 3 ML BD LUER-LOK¿ SYRINGE WITH NEEDLE LEAKED AT THE LUER CONNECTION POINT. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7697266 ↗MalfunctionJul 13, 2018Leak/Splash
IT WAS REPORTED THAT A BD ECLIPSE¿ BD LUER-LOK¿ SYRINGE WITH NEEDLE LEAKED. NO REPORTED MEDICAL INTERVENTIONS OR SERIOUS INJURY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7687790 ↗MalfunctionJul 13, 2018Leak/Splash
IT WAS REPORTED THAT THE 22 G X 1 1/2 IN. BD ECLIPSE¿ 3 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE LEAKED. THERE WAS NO REPORT OF EXPOSURE, INJURY OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7687618 ↗MalfunctionJul 13, 2018Leak/Splash
IT WAS REPORTED THAT THE 22 G X 1 1/2 IN. BD ECLIPSE¿ 3 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE LEAKED. THERE WAS NO REPORT OF EXPOSURE, INJURY OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7685757 ↗MalfunctionJul 2, 2018Leak/Splash
IT WAS REPORTED WITH THE USE OF THE BD ECLIPSE¿ BD LUER-LOK¿ SYRINGE WITH NEEDLE THERE WAS AN ISSUE WITH LEAKAGE. IT WAS STATED BY THE CONSUMER ¿THERE WAS LEAKING AT THE LUER LOCK CONNECTION WHEN PUSHING MEDS INTO THE LINE.¿ THERE WAS NO REPORT OF INJURY OR FURTHER MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7655771 ↗MalfunctionOct 25, 2017Bent
IT WAS REPORTED AFTER USE OF THE 3 ML BD SYRINGE WITH BD PRECISIONGLIDE¿ NEEDLE 25 G X 1 INCH THE NEEDLE WAS SLIGHTLY BENT AND THE HUB WAS COMING OFF THE SYRINGE. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Patient problems: No Patient Involvement
MAUDE report 6977563 ↗MalfunctionOct 25, 2017Fluid/Blood Leak
IT WAS REPORTED DURING USE OF THE 22 G X 1 1/2 IN. BD ECLIPSE¿ 3 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE FLUID WAS OBSERVED BEYOND THE RUBBER STOPPER. FLUID LEAKED BEYOND THE STOPPER. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6977557 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.