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Marpac Inc 340Recalls & reported problems

Marpac, Inc. · E-Z-Grab Endotracheal tube holder, adjustable, adult, with hydrocolloid · Class 1

Adverse event reports
1
Deaths reported
1
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00653658003406), received between Jun 10, 2022 and Jun 10, 2022 — classified as 1 death.

The most frequently reported specific device problem is “Inadequate or Insufficient Training” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Inadequate or Insufficient Training1

Patient problems

  • Unspecified Respiratory Problem1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • DeathJun 10, 2022Inadequate or Insufficient Training; Inadequate or Insufficient Training

    UNTRAINED STAFF USED THE ET TUBE HOLDER. THE RESULT WAS THAT THE ET TUBE SLIPPED. IT IS UNCLEAR WHETHER THE ET TUBE SLIPPING WAS A FACTOR CONTRIBUTING TO THE PATIENT'S DEATH OR NOT. THIS HAPPENED IN THE UK.

    Patient problems: Unspecified Respiratory Problem

    MAUDE report 14655551 ↗

Other Device, Fixation, Tracheal Tube devices

All Device, Fixation, Tracheal Tube devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.