Medline Industries, Inc. VASC1511ARecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10198459281174), received between Sep 22, 2026 and Sep 22, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (3 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 22, 2026Break; Fluid/Blood Leak

  It was reported that the female end of the tubing completely broke off causing fluid to leak.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50856908 ↗
• MalfunctionSep 22, 2026Crack; Fluid/Blood Leak

  It was reported that the female end of the tubing was cracked causing air to enter tubing and the fluid to leak.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50856483 ↗
• MalfunctionSep 22, 2026Crack; Fluid/Blood Leak

  It was reported that the female end of the tubing was cracked causing air to enter tubing and the fluid to leak.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50856074 ↗