McGRATHRecalls & reported problems across all models

We found 3 models of McGRATH by Covidien LP in the FDA's device registry (GUDID). Together they are named in 277 adverse event reports in the FDA's MAUDE database, received between Oct 16, 2019 and Sep 23, 2026 — classified as 2 deaths, 3 injuries, 272 malfunctions.

The most frequently reported specific device problem is “No Display/Image” (257 reports).

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

McGRATH recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Jan 28, 2020Open, Classified

   Blades do not fit the McGRATH MAC video laryngoscope handle or were tight fitting on the handles which may result in a change in optical performance as displayed on the video screen

   Z-1408-2020 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported McGRATH problems

McGRATH models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• McGRATH 340-000-000

  LARYNGOSCOPE, RIGID
  2 deaths192 reports
• McGRATH 340-000-000

  LARYNGOSCOPE, RIGID
  84 reports
• McGRATH X3-003-000

  LARYNGOSCOPE, RIGID
  1 recall1 report

Recent McGRATH adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionSep 23, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50874549 ↗
• MalfunctionSep 21, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50849118 ↗
• MalfunctionSep 17, 2026Temperature Problem

  It was reported that when the battery was used, the handle started to heat up. There was no patient involved.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50801780 ↗
• MalfunctionSep 16, 2026No Display/Image

  It was reported that with the battery, the handle displayed a blue screen only prior to use. The issue was not isolated to the battery. There was no patient involved.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50787153 ↗
• MalfunctionSep 15, 2026Naturally Worn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50782173 ↗
• MalfunctionSep 15, 2026No Display/Image

  It was reported that during rapid sequence induction for endotracheal intubation, the video laryngoscope exhibited a software malfunction resulting in a frozen/blocked screen. The device functioned normally during the pre-use check; however, the issue occurred at the time of intubation and was resolved after replacing the battery. A post-procedure test with the same battery reproduced the malfunction. The intubation was successfully completed, and no patient injury was reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions; Respiratory Insufficiency

  MAUDE report 50772486 ↗
• MalfunctionAug 27, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50465130 ↗
• MalfunctionAug 24, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50419813 ↗
• MalfunctionAug 24, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50419804 ↗
• MalfunctionAug 24, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50419782 ↗
• MalfunctionAug 12, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50227604 ↗
• MalfunctionAug 11, 2026Temperature Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50202629 ↗
• MalfunctionAug 8, 2026No Display/Image

  It was reported that with the battery, the handle had a blue screen not even a battery icon, and there were times when it did not light up. The issue was isolated to the battery after battery replacement was performed. There was no patient involved.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50184592 ↗
• MalfunctionAug 3, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50114254 ↗
• MalfunctionJul 16, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25842734 ↗

Other Covidien LP products

• Endo GIA48 models · 26,277 reports · 8 recalls
• Endo GIA Ultra3 models · 15,650 reports
• Shiley387 models · 9,392 reports · 5 recalls
• Signia16 models · 8,201 reports · 6 recalls
• LigaSure32 models · 7,283 reports · 1 recall
• Tri-Staple 2.037 models · 4,892 reports · 2 recalls
• Polysorb291 models · 4,564 reports · 2 recalls
• EEA39 models · 4,432 reports · 1 recall