Medline Industries, Inc. DYNJ60236CRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327680398), received between Sep 23, 2026 and Sep 23, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 23, 2026Loss of or Failure to Bond; Material Split, Cut or Torn

  It was reported that "Account is still having repeat issues with the drape. Pouch adhesive issue, Its definitely the adhesive not being strong enough. The adhesive giving way and pouches tearing off."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50872363 ↗