BD Luer-Lok, BD Eclipse 305788Recalls & reported problems
Becton, Dickinson And Company · SYRINGE 3ML LL W/NDL ECLIPSE 22X1 RB · Class 2
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00382903057887), received between Jul 12, 2018 and Nov 1, 2022 — classified as 7 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.
Most reported problems
Device problems
- Leak/Splash4
- Device Contamination with Chemical or Other Material1
- Device Markings/Labelling Problem1
- Material Deformation1
Patient problems
- No Known Impact Or Consequence To Patient6
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 1, 2022Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT FOREIGN, OIL-LIKE RESIDUE WAS FOUND ON THE PLUNGER OF THE BD ECLIPSE¿ INJECTION NEEDLE WITH LUER-LOCK¿ SYRINGE WHILE DRAWING UP MEDICATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THIS MORNING, A NURSE BROUGHT SOMETHING TO MY ATTENTION ABOUT THESE SPECIFIC BD SYRINGES. THEIR PRIMARY PURPOSE IS FOR SUBCUTANEOUS HEPARIN INJECTION. WHEN THE NURSE BEGAN TO DRAW THE MEDICATION UP INTO THE SYRINGE, SHE NOTICED AN OIL LIKE RESIDUE ON THE PLUNGER OF THE SYRINGE WHEN IT WAS PULLED BACK. WE DON¿T BELIEVE WE¿VE SEEN ANYTHING LIKE THIS ON ANY OF THE OTHER SYRINGES WE USE ON THE UNIT, SO WE WANTED TO BRING THIS FORWARD TO YOU IN CASE THIS IS SOME SORT OF DEFECT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15709760 ↗MalfunctionOct 11, 2019Leak/Splash; Leak/Splash
MATERIAL NO.: 305788 . BATCH NO.: 8302596. IT WAS REPORTED THAT DURING USE OF THE BD SYRINGE 3ML LL W/NDL ECLIPSE 22X1 RB THE SYRINGE PLUNGERS ARE HARD TO PUSH. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE PLUNGER OF SYRINGES IS HARD TO PUSH (STICKING) ITS KEEPS STOPPING AND IT NEEDS TO PUSH HARD.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9178485 ↗MalfunctionJun 25, 2019Leak/Splash; Leak/Splash
IT WAS REPORTED THAT PRIOR TO USE IT WAS NOTICED THAT THE STOPPER WAS DEFORMED WITH A BD SYRINGE 3ML LL W/NDL ECLIPSE 22X1 RB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: DISTORTED STOPPER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8732666 ↗MalfunctionMar 29, 2019Material Deformation
IT WAS REPORTED BD SYRINGE¿ 3ML LL W/NDL ECLIPSE¿ 22X1 RB HAD A DISTORTED STOPPER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8465846 ↗MalfunctionMar 26, 2019Device Markings/Labelling Problem
IT WAS REPORTED THAT A SYRINGE 3ML LL W/NDL ECLIPSE 22X1 RB HAD SCALE MARKING ERROR. THE FOLLOWING WAS REPORTED, "SCALE MISSING".
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8453791 ↗MalfunctionJul 12, 2018Leak/Splash
IT WAS REPORTED THAT THERE WAS LEAKAGE AT THE LUER CONNECTION OF THE BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE. THERE WAS NO REPORT OF EXPOSURE, INJURY, OR MEDICAL INTERVENTION NOTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7683006 ↗MalfunctionJul 12, 2018Leak/Splash
IT WAS REPORTED THAT THERE WAS LEAKAGE AT THE LUER CONNECTION OF THE BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE. THERE WAS NO REPORT OF EXPOSURE, INJURY, OR MEDICAL INTERVENTION NOTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682975 ↗
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.