Medline Industries, Inc. DYNJ44929GRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459050893), received between Sep 15, 2025 and Sep 15, 2025 — classified as 1 malfunction.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 15, 2025Contamination; Contamination

  ACCORDING TO THE FACILITY, "I IDENTIFIED A BLACK DISCOLORATION ON THE INSIDE OF A SYRINGE PRIOR TO USAGE ON (B)(6) 2025. CONCERNED IT WAS A CONTAMINATION, WE TORE DOWN ALL SETUP THAT HAD BEEN OPENED." PER THE FACILITY, "A PATIENT WAS NOT INVOLVED OR IN THE ROOM AT THE TIME; THE CASE WAS ONLY DELAYED BY 15-20 MINUTES."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23056936 ↗