Fluid Dispensing Connector 415080Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04022495820105), received between Sep 10, 2019 and Feb 7, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (3 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

Recent adverse event reports

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

• MalfunctionFeb 7, 2026Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: REPORTING A GREEN SHAVING FROM FLUID DISPENSING CONNECTOR (REF 415080) THAT WAS LOOSE AND TRANSFERRED INTO A STERILE SYRINGE FOR PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24285785 ↗
• MalfunctionJun 9, 2021Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT PARTICULATE MATTER WAS OBSERVED IN THE IMP-IV BAGS AFTER THE INFUSION WAS PREPARED. NO INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11970446 ↗
• MalfunctionSep 10, 2019Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT THE PHARMACY TECHNICIAN NOTED A BLACK SUBSTANCE ON THE GREEN TIP OF THE FLUID DISPENSING CONNECTOR AS SOON AS THE PRODUCT WAS REMOVED FROM THE PACKAGING. NO PATIENT INVOLVEMENT.

  Patient problems: No Patient Involvement

  MAUDE report 8980190 ↗