Medline Industries, Inc. VASC1459Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327509781), received between Dec 31, 2024 and Mar 20, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Connection 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 20, 2026Loose or Intermittent Connection

  IT WAS REPORTED THAT "THE CONTROL SYRINGE ROTATES OFF THE END OF THE MANIFOLD WHEN ASPIRATING/INJECTING FLUIDS" ON (B)(6) 2026. THE CUSTOMER REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT AND THAT AN ADDITIONAL CONTROL SYRINGE WAS UTILIZED TO COMPLETE THE PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24654843 ↗
• MalfunctionDec 31, 2024Connection Problem; Connection Problem

  ACCORDING TO THE FACILITY "THE CONTROL SYRINGE SUPPOSEDLY DOESN'T STAY CONNECTED WELL ENOUGH TO THE MANIFOLD ONCE ATTACHED AND LOOSENS, THEREFORE CAUSING ISSUES WITH AIR BUBBLES AND LEAKS".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21048733 ↗