Medline Industries, Inc. DYNJ62920ARecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327454753), received between Aug 10, 2026 and Sep 29, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Frayed” (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 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.

• MalfunctionSep 29, 2026Material Separation

  It was reported that towels were wrapped around the patient's aseptically prepped skin. Blue lint was observed on the patient's skin in the operating room. The patient was re-prepped, and the lint was removed.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50937005 ↗
• MalfunctionAug 10, 2026Material Frayed

  It was reported that "All blue towels are linting when surgeons use them to dry off and when they are placed on prepped patient skin."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50199678 ↗