Medline Industries, Inc. DYNJT3093Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459305801), received between Jul 25, 2025 and Jul 25, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection Problem” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Feb 27, 2026Class IOpen, Classified

   Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

   Z-1724-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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.

• MalfunctionJul 25, 2025Connection Problem; Connection Problem

  ACCORDING TO THE FACILITY, "THE SYRINGE WAS BEING CONNECTED TO THE END OF THE MANIFOLD WHERE IT IS TYPICALLY CONNECTED" AND 'ONCE THREADED ON THE MANIFOLD THE SYRINGE WILL BACK OFF OF THE MANIFOLD WHEN ANY PRESSURE IS APPLIED'.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22605687 ↗