BD EclipseTM Needle 23G x 1"TW 305826Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903058266), received between Sep 28, 2023 and Sep 30, 2024 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Defective Component” (1 report).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2024Material Separation; Material Separation

  IT WAS REPORTED THAT BD NEEDLE ECLIPSE 23X1 RB SAFETY SHIELD FELL OFF. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE ECLIPSE SAFETY NEEDLE SHIELD FELL OFF WHEN THE PACKAGING WAS OPENED AND ANOTHER TIME WHEN ACTIVATING THE SAFETY SHIELD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20334320 ↗
• MalfunctionMay 22, 2024Defective Component; Defective Component

  IT WAS REPORTED THAT THE BD ECLIPSETM NEEDLE 23G X 1"TW SAFETY MECHANISM FAILED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "WHEN ATTEMPTING TO ENGAGE SAFETY LOCK ON A 23 G NEEDLE, THE NEEDLE AND CAP DISCONNECTED FROM SYRINGE AND SAFETY DID NOT ENGAGE. NO ONE WAS INJURED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19377321 ↗
• MalfunctionSep 28, 2023Retraction Problem; Mechanical Jam; Retraction Problem; Mechanical Jam

  IT WAS REPORTED THAT THE BD ECLIPSE¿ NEEDLE SAFETY WOULD NOT ENGAGE AFTER THE INJECTION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CUSTOMER REPORTED AT THE BEDSIDE, THE NURSE WAS ADMINISTERING A VACCINE IN A 3ML SYRINGE WITH A 23 1INCH BD NEEDLE. AFTER THE INJECTION WAS COMPLETED, THE NURSE ATTEMPTED TO ENGAGE THE SAFETY TO PREVENT AN ACCIDENTAL NEEDLE STICK. THE SAFETY WOULD NOT ENGAGE. NO HARM OCCURRED DUE TO THIS EVENT. NO LOT NUMBER PROVIDED, NO WRAPPER OR DEVICE SAVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17830819 ↗

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