Medline Industries, Inc. DYNJ60113CRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327177478), received between Feb 22, 2024 and Mar 11, 2024 — classified as 2 malfunctions.

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

• MalfunctionMar 11, 2024Contamination; Contamination

  IT WAS REPORTED THAT A SYRINGE COMPONENT WAS NOTED TO HAVE BLACK STAINING WITHIN THE BARREL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18881117 ↗
• MalfunctionFeb 22, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  IT WAS REPORTED THAT AN EAR ULCER SYRINGE COMPONENT WAS "DEFECTIVE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18763995 ↗