LMA IPN042415Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05060112310577), received between Jan 7, 2022 and Jan 7, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 7, 2022Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT "THE CUSTOMER INDICATES THAT THE FASTRACH TUBE COULD NOT BE INSERTED WELL THROUGH THE FASTRACH LARYNGEAL MASK, BUT THIS WAS SOLVED BY TURNING THE TUBE 15 DEGREES". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION UNKNOWN AT TIME OF REPORT.

  Patient problems: Insufficient Information

  MAUDE report 13197934 ↗