Medline Industries, Inc. DYNJ66034BRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327680596), received between Jun 19, 2026 and Aug 14, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Frayed” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• MalfunctionAug 14, 2026Crack; Material Frayed

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50252783 ↗
• MalfunctionJun 19, 2026Material Frayed

  IT WAS REPORTED THAT THE RAYTEC USED IN THE PROCEDURES BEGAN TO FRAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25568350 ↗