Medline Industries, Inc. DYNJ07950JRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489329490), received between Aug 12, 2026 and Aug 12, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Fragmentation” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 12, 2026Material Fragmentation

  It was reported that "When the providers dry their hands on the blue towels, the towels are leaving blue lint all over the hands."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50223758 ↗