Filter Straw 415021Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04022495284129), received between Jul 3, 2018 and Mar 10, 2020 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (2 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 10, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT UPON OPENING THE FILTER STRAW TO DRAW UP FUROSEMIDE, A WHITE POWDER DEBRIS WAS NOTICED IN THE TUBE. NO INJURY REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9810566 ↗
• MalfunctionMar 10, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT UPON OPENING THE FILTER STRAW TO DRAW UP FUROSEMIDE, A WHITE POWDER DEBRIS WAS NOTICED IN THE TUBE. NO INJURY REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9810563 ↗
• MalfunctionJul 3, 2018Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  AS REPORTED BY THE USER FACILITY: CUSTOMER REPORTS THAT THE PRODUCT IS BEING FOUND WITH AN OPAQUE, MURKY WHITE SUBSTANCE ON THE BASE OF THE FILTER STRAW WHEN OPENING PACKAGE. NO PATIENT INVOLVEMENT.

  Patient problems: No Patient Involvement

  MAUDE report 7661578 ↗