Agento™ I.C.® Silver-Coated Endotracheal Tube 500390Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741067327), received between Jan 16, 2018 and Jan 16, 2018 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Inflation 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 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.

• MalfunctionJan 16, 2018Inflation Problem

  IT WAS REPORTED THAT THE AGENTO GAUGE WOULD NOT INFLATE.

  Patient problems: No Information

  MAUDE report 7196218 ↗
• MalfunctionJan 16, 2018Inflation Problem

  IT WAS REPORTED THAT THE AGENTO WOULD NOT STAY INFLATED.

  Patient problems: No Information

  MAUDE report 7195376 ↗
• MalfunctionJan 16, 2018Structural Problem; Device Operates Differently Than Expected

  IT WAS REPORTED THAT THE AGENTO WAS NOT TIGHT ENOUGH TO ENSURE EASY ACCESS DOWN THE PATIENT'S THROAT.

  Patient problems: No Information

  MAUDE report 7195375 ↗