Medline Industries, Inc. DYNJ82583Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327198183), received between Sep 11, 2026 and Sep 11, 2026 — classified as 1 malfunction.

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

• MalfunctionSep 11, 2026Material Separation

  It was reported that "The bag on the arthroscopy drape in the new ACL packs separated from the drape under the thigh, leaving an approximately 6 inch break in the sterile field."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50735461 ↗