Medline Industries, Inc. DYNJ62204Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489633474), received between Sep 3, 2019 and Sep 3, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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 3, 2019Material Fragmentation; Contamination /Decontamination Problem

  IT WAS REPORTED THAT THE GAUZE LINTED INTO THE PATIENTS EYE DURING AN UNIDENTIFIED EYE PROCEDURE.

  Patient problems: Foreign Body In Patient

  MAUDE report 8955888 ↗