Shiley 87430Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521816275), received between Oct 29, 2025 and Aug 20, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Connection Problem” (1 report).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 20, 2026Use of Device Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50359818 ↗
• MalfunctionOct 29, 2025Connection Problem; Connection Problem

  IT WAS REPORTED THAT PRIOR TO USAGE, THE ENDOTRACHEAL TUBE HAD DIFFICULTY REMOVING THE WHITE 15 MM CONNECTOR AND TUBE WAS UNUSABLE. THERE WAS NO ADDITIONAL REFERENCE ON THE PACKAGE THAT THE TUBE HAD DETACHABLE CONNECTOR, ON THE DELIVERY NOTE IT SAYS, "WITH DETACHABLE CONNECTOR". THERE WAS NO PATIENT INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23414945 ↗