Mallinckrodt 86222Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50884522005751), received between Jun 28, 2018 and Jun 28, 2018 — classified as 1 injury.

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

• InjuryJun 28, 2018Kinked; Kinked

  ACCORDING TO THE REPORTER, DURING USE, THE DEVICE HAD PHYSICAL DAMAGED. IT WAS REPORTED THAT THE TUBE BECAME SOFT EXCESSIVELY AFTER 24 HOURS OF HAVING PLACED IN THE PATIENT. THE PATIENT BEGAN TO DESATURATE BECAUSE THE TUBE COLLAPSED AND THE TUBE LIGHT WAS CLOSED. THE PHYSICIAN DECIDED TO CUT THE TUBE AT THE SECTION THAT WAS COLLAPSED BUT THEN THE TUBE COLLAPSED AGAIN IN THE NEW SECTION. THE PHYSICIAN DECIDED TO RE-INTUBATE THE PATIENT. IT WAS INDICATED THAT THE TUBE BECAME SOFT BECAUSE OF THE HEAT IN THE INCUBATOR BUT CLAIMED THAT THE PACKAGE OF THE TUBE DID NOT INDICATE THE MAXIMUM TEMPERATURE IN WHICH THE TUBE CAN BE EXPOSED.

  Patient problems: Extubate

  MAUDE report 7645899 ↗