Mallinckrodt 18760Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 50884522007571), received between Jul 31, 2017 and Aug 13, 2019 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Contamination” (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 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.

• MalfunctionAug 13, 2019Use of Device Problem; Use of Device Problem

  ACCORDING TO THE REPORTER, THE TUBE HAD CUFF INFLATION/DEFLATION ISSUE. REINTUBATION WAS REQUIRED.

  Patient problems: Extubate; No Information

  MAUDE report 8891148 ↗
• MalfunctionSep 7, 2018Material Discolored; Material Discolored

  ACCORDING TO THE REPORTER, THE DEVICE HAD A DIFFERENT TUBE COLOR WHICH IS PINK COMPARED FROM THE OTHER TUBES. THE CUSTOMER INDICATED NO PATIENT INVOLVEMENT.

  Patient problems: No Patient Involvement

  MAUDE report 7856622 ↗
• MalfunctionJul 31, 2017Contamination; Contamination

  MEDTRONIC RECEIVED A REPORT THAT PRIOR TO USE ON A PATIENT, FOREIGN MATERIAL WAS FOUND INSIDE THE PACKAGE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Patient Involvement

  MAUDE report 6756179 ↗