Medline Industries, Inc. DYNJ900369IRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327276331), received between Sep 15, 2026 and Sep 15, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Misassembled” (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 15, 2026Component Misassembled

  It was reported that the entire version "I" of the kit was setup incorrectly with the cautery pen being put outside of the sterile portion of the kit, when traditionally it has always been in the sterile portion of the kit.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50775220 ↗