Medline Industries, Inc. VASC1232Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10193489444001), received between Apr 23, 2024 and Sep 29, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Material Twisted/Bent

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50933790 ↗
• MalfunctionApr 23, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER, "PACKAGING IS CRUMPLED ON A LARGE PORTION OF THE PACKAGES. SOME PERFORATED WITH BROKEN STOPCOCKS. WHEN UNPACKING FROM BOXES THE PACKAGES THEY WERE VISIBLE CRUNCHED. WHEN OPENING ITS CONTENTS THERE WERE VISIBLY BROKEN AND BENT COMPONENTS."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19169427 ↗
• MalfunctionApr 23, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER "THE 3ML SYRINGES ARE NOT RETAINING PLUNGER PORTION WHEN PULLED BACK TO FILL. THE ENTIRE STEM SHOOTS OUT WHEN IT SHOULD HAVE A LIP INTERNALLY IN THE BARREL OF THE SYRINGE TO RETAIN THE PLUNGER PORTION".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19169426 ↗