NAMIC 60193091Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489050981), received between Dec 6, 2024 and Dec 6, 2024 — 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 16, 2026.

Recalls naming this device

1. Feb 27, 2026Open, 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-1718-2026 · 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.

• MalfunctionDec 6, 2024Connection Problem; Connection Problem

  ACCORDING TO THE FACILITY ON 11/11, "THE SYRINGE WAS CONNECTED TO THE BACK END OF THE MANIFOLD WHILE FLUSHING THE MANIFOLD IT STARTED TO UNSCREW OR BACK ITSELF OFF".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20860851 ↗