BD Luer-Lok, BD EclipseRecalls & reported problems across all models

We found 12 models of BD Luer-Lok, BD Eclipse by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 244 adverse event reports in the FDA's MAUDE database, received between Oct 25, 2017 and Sep 11, 2026 — classified as 12 injuries, 232 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (54 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported BD Luer-Lok, BD Eclipse problems

BD Luer-Lok, BD Eclipse models

12 models, most reported first. Each model has its own page with its reports, recalls and device details.

• BD Luer-Lok, BD Eclipse 305780

  Needle, hypodermic, single lumen
  50 reports
• BD Luer-Lok, BD Eclipse 305787

  Needle, hypodermic, single lumen
  49 reports
• BD Luer-Lok, BD Eclipse 305782

  Needle, hypodermic, single lumen
  47 reports
• BD Luer-Lok, BD Eclipse 305789

  Needle, hypodermic, single lumen
  28 reports
• BD Luer-Lok, BD Eclipse 305786

  Needle, hypodermic, single lumen
  16 reports
• BD Luer-Lok, BD Eclipse 305785

  Needle, hypodermic, single lumen
  14 reports
• BD Luer-Lok, BD Eclipse 305781

  Needle, hypodermic, single lumen
  12 reports
• BD Luer-Lok, BD Eclipse 305783

  Needle, hypodermic, single lumen
  12 reports
• BD Luer-Lok, BD Eclipse 305788

  Needle, hypodermic, single lumen
  7 reports
• BD Luer-Lok, BD Eclipse 305778

  Needle, hypodermic, single lumen
  5 reports
• BD Luer-Lok, BD Eclipse 305784

  Needle, hypodermic, single lumen
  3 reports
• BD Luer-Lok, BD Eclipse 305779

  Needle, hypodermic, single lumen
  1 report

Recent BD Luer-Lok, BD Eclipse adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionSep 11, 2026Break; Activation, Positioning or Separation Problem

  Patient problems: Needle Stick/Puncture

  MAUDE report 50736892 ↗
• MalfunctionApr 11, 2026Break

  IT WAS REPORTED BY CUSTOMER THAT THE NEEDLE BROKE OFF WHEN TRYING TO PULL BACK THE PLUNGER. VERBATIM: COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED WE HAVE A PATIENT THAT HAS BROUGHT A PRODUCT COMPLAINT FOR THE BD ECLIPSE 1 ML 27GX1/2 ITEMS. THEY STATED THAT THE NEEDLE BROKE OFF WHEN TRYING TO PULL BACK THE PLUNGER. WOULD YOU BE ABLE TO INVESTIGATE AND SEE IF YOU HAVE ANY OTHER COMPLAINTS WITH THIS ITEM. THE LOT# 5213561 AND THE EXPIRATION DATE IS 07/31/2030 OF THE ITEM IN QUESTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24852617 ↗
• 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 ↗
• MalfunctionDec 18, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT BD SYRINGE 3ML LL W/NDL ECLIPSE 25X1 RB LEAKED IT WAS REPORTED BY CUSTOMER THAT THEY NOTED LEAKAGE FROM HUB OF NEEDLE. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. (B)(6) MDIP REFERENCE NUMBER (ID): (B)(4). DATE OF INCIDENT (YYYY-MM-DD): (B)(6) 2025 SITE NAME/LOCATION: LEVEL OF HARM: (B)(6) OPTIONAL REPORT TO (B)(4): INCIDENT DETAILS: CLIENT CAME TO CLINIC FOR INFLUENZA VACCINE. DURING IMMUNIZATION TO PATIENT'S LEFT ARM AT 17:25HRS WRITER NOTED LEAKAGE FROM HUB OF NEEDLE. WRITER INFORMED (B)(6), WRITER ADVISED TO READMINISTER VACCINE AS PATIENT DID NOT RECEIVE A FULL DOSE. WRITER EXPLAINED THIS TO THE PATIENT, PATIENT AGREEABLE TO HAVE THE FLU VACCINE RE ADMINISTERED. WRITER READMINISTERED A SECOND INFLUENZA VACCINE TO RIGHT ARM AND IMMUNIZATION WAS EFFECTIVE. CLIENT UNDERSTANDING OF SITUATION. IMPACT OF INCIDENT: WHO WAS AFFECTED? PATIENT FREQUENCY OF PROBLEM: OTHER DEVICE/INCIDENT FACTORS: INVASIVE PROCEDURE? PROCEDURE: RESULTED IN A DOUBLE POKE FOR A PATIENT PHYSICIAN: DEVICE INFORMATION DEVICE NAME/DESCRIPTION: SYRINGE 3ML WITH NEEDLE SAFETY 25GA X 1 IN MANUFACTURER: BECTON DICKINSON CANADA INC MANUFACTURER CODE/MODEL: 305787 SERIAL OR L

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23842690 ↗
• MalfunctionOct 15, 2025Nonstandard Device; Defective Component; Nonstandard Device; Defective Component

  WHEN USED FOR BLOOD DRAWING THE SYRINGE STOPPER IS DEFORMED, CAUSING THE SAMPLE TO LEAK OUT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23300364 ↗
• MalfunctionJul 2, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT BD SYRINGE 3ML LL W/NDL ECLIPSE 23X1 RB LEAKED AT LUER CONNECTION IT WAS REPORTED BY CUSTOMER THAT BD ECLIPSE 3ML 23G X 1IN LEAKS WHEN LUER-LOK ATTACHED TO IV CATHETER. RCC RECEIVED A COMPLAINT VIA EMAIL. BD ECLIPSE 3ML 23G X 1IN LEAKS WHEN LUER-LOK ATTACHED TO IV CATHETER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22384632 ↗
• 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 ↗
• MalfunctionMay 22, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD SYRINGE 3ML LL W/NDL ECLIPSE 23X1 RB HAD LEAKAGE AT THE LUER CONNECTION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 305782 , BATCH # 4187641. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. WE HAVE RECEIVED A QUALITY COMPLAINT ON PRODUCT SOLD TO OUR CUSTOMER. PLEASE CONTACT THE CUSTOMER, AND INCLUDE COMPLAINT# (B)(4) ON ANY FUTURE COMMUNICATIONS. INJURIES OR ADVERSE EVENT: NO. ITEM: 305782. QUANTITY AFFECTED:1CS. SERIAL/LOT NUMBER: (B)(6). PO : (B)(6). ARE ANY SAMPLES AVAILABLE FOR RETURN? YES. REPORTED ISSUE: THE ITEM IS LEAKING WHEN ATTACHED TO AN EXTENSION SET; LEAKING WHERE LUER CONNECTOR MEETS THE SET. THIS IS HAPPENING ON ONLY THIS SYRINGE AND ISSUE DOES NOT OCCUR WHEN USING A DIFFERENT PRODUCT FROM BD. CUSTOMER DISPOSITION REQUEST: REPLACEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22075200 ↗
• MalfunctionFeb 21, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

  NO ADDITIONAL INFORMATION

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21434309 ↗
• MalfunctionJan 15, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 27X1/2 RB LEAKED. IT WAS REPORTED BY CUSTOMER THAT CLINICIANS ARE SAYING THEY ARE LEAKING. I DO NOT HAVE A SAMPLE TO TURN IN. RCC RECEIVED A COMPLAINT VIA EMAIL. CLINICIANS ARE SAYING THEY ARE LEAKING. I DO NOT HAVE A SAMPLE TO TURN IN. ITEM: 305789 QUANTITY AFFECTED: 2 EA SERIAL/LOT NUMBER: N/A PO: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21158587 ↗
• MalfunctionJan 6, 2025Leak/Splash; Leak/Splash

  MATERIAL# 305787, BATCH# 4084135. IT WAS REPORTED BY CUSTOMER THAT HE IS USING ITEM 305787; LOT 4084135 AND THE PLUNGER IS SLIGHTLY BENT AND THE PLUNGER IS HARD TO PUSH. HE PUSHES THE PLUNGER HARD TO GET THE MEDICATION TO DELIVER AND THEN HE ENDS UP LOSING MEDICATION BECAUSE OF THE FORCE IT TAKES TO PUSH THE PLUNGER. HE HAS ABOUT 1/2 OF A BOX LEFT AND WOULD LIKE REPLACEMENTS. VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. CUSTOMER STATES THAT HE IS USING ITEM 305787; LOT 4084135 AND THE PLUNGER IS SLIGHTLY BENT AND THE PLUNGER IS HARD TO PUSH. HE PUSHES THE PLUNGER HARD TO GET THE MEDICATION TO DELIVER AND THEN HE ENDS UP LOSING MEDICATION BECAUSE OF THE FORCE IT TAKES TO PUSH THE PLUNGER. HE HAS ABOUT 1/2 OF A BOX LEFT AND WOULD LIKE REPLACEMENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21086686 ↗
• MalfunctionDec 30, 2024Complete Blockage; Complete Blockage

  MATERIAL#: 305787, BATCH NUMBER#: 1301551. IT WAS REPORTED BY CUSTOMER THAT BATCH OF NEEDLE HAVE A LOT OF RESISTANCE VERBATIM#: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. BATCH OF NEEDLE HAVE A LOT OF RESISTANCE. REF: (B)(4). LOT: 1301551. HAS SAMPLES AVAILABLE FOR INVESTIGATION, WOULD LIKE A REPLACEMENTS FOR BOX.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21037174 ↗
• 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 ↗

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