Medline Industries, Inc. DYNJ0718669CRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942208852), received between Dec 21, 2017 and Dec 21, 2017 — classified as 1 malfunction.

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

• MalfunctionDec 21, 2017Fire

  IT WAS REPORTED THAT THERE WAS AN ARCH DURING A CASE AND IT CAUSED A SMALL FIRE. THE FIRE WAS PUT OUT RIGHT AWAY WITH NO PATIENT IMPACT AND NO PROPERTY DAMAGE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7137663 ↗