Medline Industries, Inc. DYNJ86576Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10195327652395), received between Apr 1, 2026 and Sep 14, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 14, 2026Fluid/Blood Leak

  It was reported that a betadine bottle leaked within the pack.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50756634 ↗
• MalfunctionApr 3, 2026Dull, Blunt

  ACCORDING TO THE FACILITY ON (B)(6) 2026, "WHEN TRYING TO THE USE #15 BLADE DURING THE SURGERY, THE BLADE WAS SO DULL THAT IT WAS BARELY CUTTING THE SKIN."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24779985 ↗
• MalfunctionApr 1, 2026Dull, Blunt

  ACCORDING TO THE FACILITY ON (B)(6) 2026, "WHEN TRYING TO THE USE #15 BLADE, DURING THE SURGERY, THE BLADE WAS SO DULL THAT IT WAS BARELY CUTTING THE SKIN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24758159 ↗