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McGRATH MAC 350-005-000 (UDI 10884521816312)Recalls & reported problems

Covidien LP · Disposable Laryngoscope Blade 3 · Class 1

Adverse event reports
19
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 19 adverse event reports that list this exact device (DI 10884521816312), received between Dec 8, 2023 and Jan 15, 2025 — classified as 19 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (13 reports).

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 2 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 6 reportsApr 2024: 5 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 1 reportsOct 2024: 0 reportsNov 2024: 2 reportsDec 2024: 0 reportsJan 2025: 3 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520266
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Electrical /Electronic Property Problem13
  • Material Opacification6

Patient problems

  • No Clinical Signs, Symptoms or Conditions19

Recent adverse event reports

The 19 most recent of 19 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 15, 2025Material Opacification; Material Opacification

    IT WAS REPORTED THAT THREE MCGRATH MAC 3 BLADE WAS FOGGY BEFORE USE AT A HOSPITAL. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21155462 ↗
  • MalfunctionJan 15, 2025Material Opacification; Material Opacification

    IT WAS REPORTED THAT THREE MCGRATH MAC 3 BLADE WAS FOGGY BEFORE USE AT A HOSPITAL. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21155413 ↗
  • MalfunctionJan 15, 2025Material Opacification; Material Opacification

    IT WAS REPORTED THAT THREE MCGRATH MAC 3 BLADE WAS FOGGY BEFORE USE AT A HOSPITAL. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21155410 ↗
  • MalfunctionNov 15, 2024Material Opacification; Material Opacification

    ACCORDING TO THE REPORTER, PRIOR TO USAGE, THE 2 VIDEO LARYNGOSCOPE'S BLADES WERE FOUND BLURRY. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20695951 ↗
  • MalfunctionNov 15, 2024Material Opacification; Material Opacification

    ACCORDING TO THE REPORTER, PRIOR TO USAGE, THE 2 VIDEO LARYNGOSCOPE'S BLADES WERE FOUND BLURRY. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20695931 ↗
  • MalfunctionSep 9, 2024Material Opacification; Material Opacification

    ACCORDING TO THE REPORTER, PRIOR TO USE, THERE WAS A MOISTURE OCCURRENCE IN THE BLADE OF THE VIDEOLARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20167756 ↗
  • MalfunctionApr 2, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE FOUND FROM EACH OF THE VIDEO LARYNGOSCOPE'S BLADES. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19020517 ↗
  • MalfunctionApr 2, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE FOUND FROM EACH OF THE VIDEO LARYNGOSCOPE'S BLADES. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19020475 ↗
  • MalfunctionApr 2, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE FOUND FROM EACH OF THE VIDEO LARYNGOSCOPE'S BLADES. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19020380 ↗
  • MalfunctionApr 2, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE FOUND FROM THE VIDEO LARYNGOSCOPE'S BLADE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19020298 ↗
  • MalfunctionApr 2, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE FOUND FROM EACH OF THE VIDEO LARYNGOSCOPE'S BLADES. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19020218 ↗
  • MalfunctionMar 27, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE GENERATED IN THE VIDEOLARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18988750 ↗
  • MalfunctionMar 27, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE GENERATED IN THE FOUR REPORTED VIDEOLARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18988454 ↗
  • MalfunctionMar 27, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE GENERATED IN THE FOUR REPORTED VIDEOLARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18988326 ↗
  • MalfunctionMar 27, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE GENERATED IN THE VIDEO LARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18986371 ↗
  • MalfunctionMar 27, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE GENERATED IN THE FOUR REPORTED VIDEOLARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18985955 ↗
  • MalfunctionMar 27, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THERE WAS MOISTURE GENERATED IN THE FOUR REPORTED VIDEOLARYNGOSCOPE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18985907 ↗
  • MalfunctionDec 8, 2023Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THE VIDEO LARYNGOSCOPE'S BLADES HAD FOG DURING THE INTUBATION. THERE WAS NO PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18293441 ↗
  • MalfunctionDec 8, 2023Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    ACCORDING TO THE REPORTER, THE VIDEO LARYNGOSCOPE'S BLADES HAD FOG DURING THE INTUBATION. THERE WAS NO PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18293427 ↗

Other LARYNGOSCOPE, RIGID devices

All LARYNGOSCOPE, RIGID devices →

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