BD Eclipse Needle 25G x 1 1/2 TW 305838Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00382903058389), received between Jun 21, 2024 and Feb 18, 2025 — classified as 1 injury, 4 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (4 reports).

1 other recall cover devices cleared under the same FDA submission (K161170); they may or may not involve this specific model.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 18, 2025Complete Blockage; Complete Blockage

  SAMPLES RECEIVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21404810 ↗
• MalfunctionSep 18, 2024Complete Blockage; Complete Blockage

  MATERIAL #:305838. BATCH#:2355495. IT WAS REPORTED THAT THE BD NEEDLE ECLIPSE 25X1-1/2 RB NEEDLE WAS CLOGGED / BLOCKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: WE HAVE HAD AN ISSUE WITH SOME 25G NEEDLES. ON 3 SEPARATE OCCASIONS THE NEEDLES HAVE CLOGGED, AND THE INJECTION WAS NOT ABLE TO BE COMPLETED. THE PATIENT UNFORTUNATELY HAD TO BE STUCK A SECOND TIME. THE NEEDLES ARE AL THE SAME LOT NUMBER, SO WE PULLED THEM FROM THE SHELF UNTIL WE HAD A PLAN OF ACTION. ADDITIONAL INFORMATION PROVIDED: I NOTICED THE EMAIL STATES THAT WE ARE AT (B)(6), WE ARE (B)(6) HOSPITAL IN (B)(6). THE INCIDENT OCCURRED ONE TIME ON 08/01/2024 AND THEN OCCURRED TWICE ON 08/20/2024. THE LOT NUMBER IS 2355495, NO OTHER LOTS ARE AFFECTED. A SHIPPING LABEL CAN BE SENT TO: (B)(6).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20248323 ↗
• MalfunctionSep 18, 2024Complete Blockage; Complete Blockage

  MATERIAL #:305215. BATCH#:2355495. IT WAS REPORTED THAT THE BD NEEDLE ECLIPSE 25X1-1/2 RB NEEDLE WAS CLOGGED / BLOCKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY CUSTOMER THAT THEY HAD AN ISSUE WITH SOME 25G NEEDLES. ON 3 SEPARATE OCCASIONS THE NEEDLES HAVE CLOGGED, AND THE INJECTION WAS NOT ABLE TO BE COMPLETED. THE PATIENT UNFORTUNATELY HAD TO BE STUCK A SECOND TIME. THE NEEDLES ARE AL THE SAME LOT NUMBER, SO WE PULLED THEM FROM THE SHELF UNTIL WE HAD A PLAN OF ACTION. ADDITIONAL INFORMATION PROVIDED: I NOTICED THE EMAIL STATES THAT WE ARE AT (B)(6). THE INCIDENT OCCURRED ONE TIME ON (B)(6) 2024 AND THEN OCCURRED TWICE ON (B)(6) 2024. THE LOT NUMBER IS 2355495, NO OTHER LOTS ARE AFFECTED. PLEASE SEE THE PICTURES BELOW. A SHIPPING LABEL CAN BE SENT TO: (B)(6).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20248315 ↗
• MalfunctionAug 25, 2024Complete Blockage; Complete Blockage

  MATERIAL: 305838 BATCH#: 2355492. IT WAS REPORTED THAT THE BD NEEDLE ECLIPSE 25X1-1/2 RB NEEDLE WAS CLOGGED/BLOCKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. VERBATIM: EVENT DATE: 8-7-2024 EVENT LOCATION: XXXX EVENT DESCRIPTION: ¿WHILE PA WAS COMPLETING A JOINT INJECTION ON A PATIENT, THE NEEDLE WOULDN'T ALLOW THE MEDICINE TO INJECT. SHE CHANGED OUT NEEDLES TO ANOTHER NEW ONE AND IT DID THE SAME THING AGAIN. NEEDLE 25 G X 1 1/2" BD ECLIPSE NEEDLE LOT 2355492 EXP 12/31/2027¿ HARM TO TEAM MEMBER OR PATIENT? NO INJURY TO MY KNOWLEDGE. PRODUCT NAME: ITM-1150133 - NEEDLE SAFETY 25G X 1.5 PRODUCT REF: 305838 LOT NUMBER: 2355492 BD CUSTOMER ACCOUNT NUMBER: (B)(6). ACTUAL PRODUCT INVOLVED IS NOT YET AVAILABLE FOR RETURN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20060865 ↗
• InjuryJun 21, 2024Activation Problem; Activation Problem

  MATERIAL# 305838 BATCH# UNKNOWN IT WAS REPORTED THAT THE BD NEEDLE ECLIPSE 25X1-1/2 RB HAS A SAFETY MECHANISM FAILURE. THE FOLLOWING INFORMATION WAS REPORTED BY THE INITIAL REPORTER: "A PATIENT SAFETY REPORT WAS SUBMITTED BY A CLINICAL STAFF MEMBER AT MOUNTAIN HOME FOR THE BD ECLIPSE NEEDLE, 25G X 1 ½¿, PART NUMBER 305838, REPORTING A DELAYED SAFETY ENGAGEMENT FOR THIS NEEDLE. ARE YOU AWARE OF ANY OTHER REPORTED QUALITY OR SAFETY ISSUES WITH THIS PRODUCT?" ADDITIONAL INFORMATION PROVIDED: THE NURSE THAT WAS STUCK DOES NOT KNOW THE LOT #. NO PT HARM. NURSE WAS STUCK AND BOTH THE PT AND NURSE HAD LABS DRAWN. I DON¿T HAVE ANY OTHER COMPLAINTS OF ISSUES WITH THE PRODUCT SO NO SAMPLE IS AVAILABLE.

  Patient problems: Needle Stick/Puncture

  MAUDE report 19581750 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K161170. One submission often covers many models, so check the product and lot details in each record.

• Z-1440-2017 · Dec 20, 2016 · Terminated
  Eclipse Hypodermic Needle