Medline Industries, Inc. DYNJ04078Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196846672), received between Sep 24, 2026 and Sep 28, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 28, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50922075 ↗
• MalfunctionSep 24, 2026Product Quality Problem; Component Missing

  It was reported that "The drape that comes in the tray is a foam drape that does not lay flat," "there is not a safety scalpel in the kit. It has a cap," and "the clamp that comes in the kit does not clamp correctly."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50889423 ↗