BD Luer-Lok, BD Eclipse 305780Recalls & reported problems

Summary

The FDA's MAUDE database contains 50 adverse event reports that list this exact device (DI 00382903057801), received between Dec 29, 2017 and Mar 31, 2026 — classified as 50 malfunctions.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (9 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 50 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 31, 2026Contamination /Decontamination Problem

  IT WAS REPORTED BY THE CUSTOMER THAT ECLIPSE NEEDLES HAVE SOME WHITE MATERIAL ON THE BASE OF THE NEEDLE. COMPLAINT VIA EMAIL. I NOTICED MY RECENTLY ORDERED BD ECLIPSE NEEDLES HAVE SOME WHITE MATERIAL ON THE BASE OF THE NEEDLE, TO THE POINT THAT IT WOULD BE INSERTED UNDER THE SKIN FOR E.G. A SUBCUTANEOUS INJECTION. I HAVE ATTACHED SOME PHOTOS. COULD YOU PLEASE CLARIFY WHETHER THIS IS NORMAL OR NOT?

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24744852 ↗
• MalfunctionMar 30, 2026Contamination /Decontamination Problem

  IT WAS REPORTED BY CUSTOMER THAT THEY ORDERED BD ECLIPSE NEEDLES HAVE SOME WHITE MATERIAL ON THE BASE OF THE NEEDLE, TO THE POINT THAT IT WOULD BE INSERTED UNDER THE SKIN. VERBATIM: COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED I NOTICED MY RECENTLY ORDERED BD ECLIPSE NEEDLES HAVE SOME WHITE MATERIAL ON THE BASE OF THE NEEDLE, TO THE POINT THAT IT WOULD BE INSERTED UNDER THE SKIN FOR E.G. A SUBCUTANEOUS INJECTION. I HAVE ATTACHED SOME PHOTOS. COULD YOU PLEASE CLARIFY WHETHER THIS IS NORMAL OR NOT?.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24729614 ↗
• MalfunctionJan 28, 2026Contamination /Decontamination Problem

  IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 25X5/8 RB HAD FOREIGN MATTER IT WAS REPORTED BY THE CUSTOMER THAT PARTICULAR NEEDLE WHEN I OPENED THE PACKAGE. THERE APPEARS TO BE A BLOB OF SOME SORT OF OIL OR A TARLIKE SUBSTANCE INSIDE THE SYRINGE. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. MY NAME IS (B)(6) AND I HAVE BEEN USING YOUR PRODUCTS FOR MY TRT THERAPY FOR A LONG TIME NOW. I AM WRITING TO INFORM YOU OF POTENTIAL PRODUCT CONTAMINATION ON SOME OF YOUR BD ECLIPSE 1ML 25G X 5/8 NEEDLES. I NOTICED SOMETHING OFF WITH THIS PARTICULAR NEEDLE WHEN I OPENED THE PACKAGE. THERE APPEARS TO BE A BLOB OF SOME SORT OF OIL OR A TARLIKE SUBSTANCE INSIDE THE SYRINGE. ATTACHED ARE SOME PHOTOS SHOWING LOT NUMBER, ISSUE AND THE INVOICE FOR THE PRODUCTS WHEN I PURCHASED THEM. I HAVE NEVER NOTICED THIS BEFORE BUT IT IS QUITE CONCERNING HAVING AN UNKNOWN SUBSTANCE INSIDE A SYRINGE THAT IS SUPPOSED TO BE STERILE. I WILL INSPECT THE SYRINGES CLOSER BEFORE EACH USE GOING FORWARD. I WANTED TO LET SOMEONE KNOW WHAT I FOUND IN HOPES IT CAN BE INVESTIGATED AND THE CONTAMINATION ISSUE RESOLVED. MY PHONE NUMBER IS (B)(6) SHOULD YOU HAVE ANY FURTHER QUESTIONS. ALSO, I AM STILL IN

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24201380 ↗
• MalfunctionJul 1, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

  IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 25X5/8 RB HAD FOREIGN MATTER THERE IS CONTAMINATION INSIDE THE SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22371671 ↗
• MalfunctionDec 29, 2024Partial Blockage; Partial Blockage

  MATERIAL #: 305780 BATCH#: 4206669. IT WAS REPORTED BY CUSTOMER THAT THEY ARE RANDOMLY NOT EXPELLING ALL THE MEDICATION OUT OF THE SYRINGE. VERBATIM: COMPLAINT RECEIVED VIA EMAIL(S) ATTACHED. EMAIL FROM MCKESSON DISTRIBUTOR REPRESENTATIVE: "I HAVE A CUSTOMER WITH A SERIOUS PROBLEM WITH BD SYRINGES. THEY ARE RANDOMLY NOT EXPELLING ALL THE MEDICATION OUT OF THE SYRINGE. I HAVE CALLED BD WITH ALL THIS ELECTRONIC RESPONSES IS A WORTHLESS WASTE OF TIME FOR ME. I HAVE BEEN TRYING TO CONNECT VIA PHONE 2 TIMES THEY DISCONNECT ME AND BY THE CHAT ON THE WEBSITE AND THEY JUST DISCONNECT ME. THE CUSTOMER IS...".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21032720 ↗
• MalfunctionSep 6, 2024Break; Break

  IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 25X5/8 RB SAFETY MECHANISM FAILED. IT WAS REPORTED BY CUSTOMER THAT IT SEEMS THAT WE HAVE NEW HEPARIN SYRINGES. A NURSE HAD TOLD ME SHE USED A HEPARIN SYRINGE AND IN ATTEMPTING ENGAGE THE SAFETY MECHANISM, IT FAILED AND BROKE OFF. THE SAFETY MECHANISM BREAKS OFF AT THE HINGE. LET ME KNOW IF YOU NEED MORE INFORMATION FROM ME. VERBATIM: COMPLAINT RECEIVED VIA EMAIL(S) ATTACHED. "IT SEEMS THAT WE HAVE NEW HEPARIN SYRINGES. A NURSE HAD TOLD ME SHE USED A HEPARIN SYRINGE AND IN ATTEMPTING ENGAGE THE SAFETY MECHANISM, IT FAILED AND BROKE OFF. THE SAFETY MECHANISM BREAKS OFF AT THE HINGE. LET ME KNOW IF YOU NEED MORE INFORMATION FROM ME."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20163731 ↗
• MalfunctionMay 10, 2024Material Protrusion/Extrusion; Material Protrusion/Extrusion

  IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 25X5/8 RB NEEDLE THROUGH SHIELD. IT WAS REPORTED BY CUSTOMER THAT PACKAGE HAD AN EXTRA EXPOSED NEEDLE STICKING OUT OF THE SEALED PACKAGE. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. SATURDAY EVENING CUSTOMER WENT TO DRAW UP HEPARIN AND THE PACKAGE HAD AN EXTRA EXPOSED NEEDLE STICKING OUT OF THE SEALED PACKAGE, CLEAN NEEDLE HOWEVER SHE ALMOST GOT STUCK.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19288175 ↗
• MalfunctionMar 22, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem

  MATERIAL#: 305780, BATCH#: UNKNOWN. IT WAS REPORTED BY THE CUSTOMER THAT THEY RECEIVED A NUMBER OF BD ECLIPSE 1ML 5/8¿ 25G SYRINGES (REF 305780) THAT HAD WORN OFF MARKINGS AND COULD NOT BE USED. I HAVE ATTACHED PICTURES OF A FEW OF THE IMPACTED SYRINGES WHERE YOU CAN SEE THE MARKINGS MISSING. UNFORTUNATELY THE PATIENT WAS UNABLE TO PROVIDE A LOT/EXPIRATION DATE FOR THESE SYRINGES AS THEY HAD PLACED THE PACKAGING IN THEIR SHARPS CONTAINER. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. WE RECEIVED THE FOLLOWING COMPLAINT REGARDING ITEM#305780 SYRINGE/NDL, ECLIPSE SAFETY 1C C THIN WALL 25GX5/8" (50/BX) FOR A TOTAL OF ONE CASE. PER THE CUSTOMER, " THEY STATED THAT THEY RECEIVED A NUMBER OF BD ECLIPSE 1ML 5/8¿ 25G SYRINGES (REF 305780) THAT HAD WORN OFF MARKINGS AND COULD NOT BE USED. I HAVE ATTACHED PICTURES OF A FEW OF THE IMPACTED SYRINGES WHERE YOU CAN SEE THE MARKINGS MISSING. UNFORTUNATELY THE PATIENT WAS UNABLE TO PROVIDE A LOT/EXPIRATION DATE FOR THESE SYRINGES AS THEY HAD PLACED THE PACKAGING IN THEIR SHARPS CONTAINER." PLEASE SEE ATTACHED PICTURES. THE ITEMS WERE PURCHASED ON PO#(B)(4). THE CUSTOMER IS REQUESTING REPLACEMENT OF THE CASE. YOU WILL FIND THE PO

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18959444 ↗
• MalfunctionMar 22, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem

  MATERIAL#: 305780, BATCH#: UNKNOWN. IT WAS REPORTED BY THE CUSTOMER THAT THEY RECEIVED A NUMBER OF BD ECLIPSE 1ML 5/8¿ 25G SYRINGES (REF 305780) THAT HAD WORN OFF MARKINGS AND COULD NOT BE USED. I HAVE ATTACHED PICTURES OF A FEW OF THE IMPACTED SYRINGES WHERE YOU CAN SEE THE MARKINGS MISSING. UNFORTUNATELY THE PATIENT WAS UNABLE TO PROVIDE A LOT/EXPIRATION DATE FOR THESE SYRINGES AS THEY HAD PLACED THE PACKAGING IN THEIR SHARPS CONTAINER. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. WE RECEIVED THE FOLLOWING COMPLAINT REGARDING ITEM#305780 SYRINGE/NDL, ECLIPSE SAFETY 1C C THIN WALL 25GX5/8" (50/BX) FOR A TOTAL OF ONE CASE. PER THE CUSTOMER, " THEY STATED THAT THEY RECEIVED A NUMBER OF BD ECLIPSE 1ML 5/8¿ 25G SYRINGES (REF 305780) THAT HAD WORN OFF MARKINGS AND COULD NOT BE USED. I HAVE ATTACHED PICTURES OF A FEW OF THE IMPACTED SYRINGES WHERE YOU CAN SEE THE MARKINGS MISSING. UNFORTUNATELY THE PATIENT WAS UNABLE TO PROVIDE A LOT/EXPIRATION DATE FOR THESE SYRINGES AS THEY HAD PLACED THE PACKAGING IN THEIR SHARPS CONTAINER." PLEASE SEE ATTACHED PICTURES. THE ITEMS WERE PURCHASED ON PO#(B)(4). THE CUSTOMER IS REQUESTING REPLACEMENT OF THE CASE. YOU WILL FIND THE PO

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18959433 ↗
• MalfunctionDec 8, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 25X5/8 RB SCALE MARKINGS MISSING THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER; IT WAS REPORTED BY CUSTOMER THAT ALLERGY NURSE PROCEED TO INJECT MEDICATION, OPENING THE BOX SHE REALIZED THAT THERE WAS NO MARKINGS ON THE SYRINGE TO DRAW THE MEDICATION. SOME OF THE SYRINGE HAD THEIR MARKING LOOKING LIKE THEY WERE RUBBED OFF. MAT# 305780 LOT 0206544, CUSTOMER ADVISED EVENT WAS REPORTED TO MCKESSON REP IN OCTOBER, AND A FOLLOW UP WAS MADE OCTOBER 24TH. MCKESSON REP ADVISED CUSTOMER TO REACH OUT TO BD DIRECTLY. VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. ALLERGY NURSE PROCEED TO INJECT MEDICATION, OPENING THE BOX SHE REALIZED THAT THERE WAS NO MARKINGS ON THE SYRINGE TO DRAW THE MEDICATION. SOME OF THE SYRINGE HAD THEIR MARKING LOOKING LIKE THEY WERE RUBBED OFF. MAT# 305780 LOT 0206544, CUSTOMER ADVISED EVENT WAS REPORTED TO MCKESSON REP IN OCTOBER, AND A FOLLOW UP WAS MADE OCTOBER 24TH. MCKESSON REP ADVISED CUSTOMER TO REACH OUT TO BD DIRECTLY.

  Patient problems: Insufficient Information

  MAUDE report 18297805 ↗
• MalfunctionMar 15, 2023Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE WITH SYRINGE EXPERIENCED LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: SYRINGE LEAKAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16547508 ↗
• MalfunctionJan 28, 2023Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT 3 OF THE BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGE HAD DIFFICULT PLUNGER MOVEMENT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM MANDARIN CHINESE TO ENGLISH: PLUNGER IS HARD TO PUSH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16261190 ↗
• MalfunctionJan 28, 2023Break; Break

  IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGE HAD A BROKEN PLUNGER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM MANDARIN CHINESE TO ENGLISH: BROKEN PLUNGER (PIR3031744)

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16261149 ↗
• MalfunctionJan 28, 2023Contamination; Contamination

  IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGE EXPERIENCED FOREIGN MATTER IN THE BARREL. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM MANDARIN CHINESE TO ENGLISH: THERE ARE FOREIGN MATTER IN THE BARREL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16261145 ↗
• MalfunctionJan 24, 2023Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT 2 BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGES HAD DIFFICULT PLUNGER MOVEMENT DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "PLUNGERS IS HARD TO PUSH"

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16236831 ↗
• MalfunctionOct 29, 2022Break; Break

  IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE 25 G X 5/8 IN. WITH DETACHABLE 1 ML BD LUER-LOK¿ SYRINGE EXPERIENCED A BROKEN BARREL. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: BROKEN BARREL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15694966 ↗
• MalfunctionOct 27, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED WHILE USING BD ECLIPSE¿ NEEDLE 25 G X 5/8 IN. WITH DETACHABLE 1 ML BD LUER-LOK¿ SYRINGE THE PLUNGER MOVEMENT WAS DIFFIECULT. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: COMPLAINT: THEY LAST ORDER THE CUSTOMER RECEIVED THEY HAVE ISSUE WITH, THE BARREL IS JAMMED AND CANNOT INJECT SECOND HALF OF THE DOSE WHEN THEY DEPRESS THE SYRINGE.

  Patient problems: Insufficient Information

  MAUDE report 15686621 ↗
• MalfunctionJun 3, 2022Break; Break

  IT WAS REPORTED WHILE USING BD ECLIPSE¿ NEEDLE 25 G X 5/8 IN. WITH DETACHABLE 1 ML BD LUER-LOK¿ SYRINGE THE PLUNGER BROKE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PLUNGER BROKEN. INCIDENT OCCUR: BEFORE USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14596593 ↗
• MalfunctionMay 11, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE STOPPER WAS FOUND MISALIGNED ON THE BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGE PLUNGER BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "DISTORTED STOPPER INCIDENT OCCUR : BEFORE USE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14356512 ↗
• MalfunctionMay 11, 2022Defective Device; Defective Device

  IT WAS REPORTED BD LUER-LOK¿ SYRINGE WITH BD ECLIPSE¿ NEEDLE HAD A DEFECTIVE STOPPER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "DISTORTED STOPPER. INCIDENT OCCUR: BEFORE USE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14354952 ↗
• MalfunctionApr 18, 2022Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE STOPPER IN THE BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGE WAS DEFECTIVE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "DISTORTED STOPPER".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14136319 ↗
• MalfunctionApr 18, 2022Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE STOPPERS IN 2 BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGES WERE DEFECTIVE/DAMAGED. THIS COMPLAINT WAS CREATED TO CAPTURE THE 1ST OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "DISTORTED STOPPER".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14135141 ↗
• MalfunctionApr 18, 2022Volume Accuracy Problem; Volume Accuracy Problem

  IT WAS REPORTED THAT THE SCALE MARKINGS ON 2 BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGES WERE ILLEGIBLE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 2ND OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "SCALE BLUR."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14135008 ↗
• MalfunctionMar 30, 2022Volume Accuracy Problem; Volume Accuracy Problem

  IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE WITH DETACHABLE BD LUER-LOK¿ SYRINGE SCALE MARKINGS WERE BLURRED TOGETHER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "SCALE BLUR".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13956813 ↗
• MalfunctionMar 29, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT THE BD ECLIPSE¿ SAFETY NEEDLES BD ECLIPSE¿ NEEDLE PLUNGER WAS DIFFICULT TO PUSH. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "PLUNGER IS HARD TO PUSH".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13934926 ↗