MEDLINE INDUSTRIES, INC. VASC1782Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459374869), received between Jan 12, 2026 and Jan 12, 2026 — classified as 1 malfunction.

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

• MalfunctionJan 12, 2026Connection Problem

  IT WAS REPORTED THAT ON (B)(6) 2025, THE "CONTROL SYRINGE ROTATES OFF THE END OF THE MANIFOLD WHEN ASPIRATING/INJECTING FLUIDS" AND "WOULDN'T STAY CONNECTED." THE CUSTOMER SAID THAT THERE WAS NO PATIENT INVOLVEMENT AND THAT THE PROCEDURE WAS ABLE TO BE COMPLETED BY OPENING "ANOTHER VASC1782 KIT AND THE CONTROL SYRINGE IN IT WORKED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24036686 ↗