Medline Industries, Inc. MDS0425615Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942563708), received between Aug 2, 2022 and Aug 30, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryAug 30, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON (B)(6) 2022 WHEN ATTEMPTING TO INTUBATE THE PATIENT FOR A PROCEDURE THE ANESTHESIA PROVIDER INSERTED THE LARYNGOSCOPE BLADE INTO THE PATIENT'S MOUTH AND WHEN THEY WENT TO LIFT UP ON THE HANDLE TO VISUALIZE THE AIRWAY THE HANDLE BROKE APART.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 15324525 ↗
• InjuryAug 2, 2022Break

  IT WAS REPORTED THAT THE LARYNGOSCOPE BROKE DURING INTUBATION. THE FACILITY REPORTED THAT THEY DID NOT HAVE ANY OF THE PATIENT OR INCIDENT DETAILS HOWEVER THERE WAS NO PATIENT INJURY NOTED, AND ANOTHER DEVICE WAS ABLE TO BE UTILIZED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15153588 ↗