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VascuTrak® V143040Recalls & reported problems

Bard Peripheral Vascular, Inc. · VascuTrak® PTA Dilatation Catheter 3 mm x 40 mm, 140 cm catheter · Class 2

All models of VascuTrak (20)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741061318), received between May 5, 2021 and May 5, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

Device problems

  • Break1
  • Detachment of Device or Device Component1
  • Difficult to Remove1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1

Recent adverse event reports

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

  • InjuryMay 5, 2021Break; Difficult to Remove; Detachment of Device or Device Component; Break; Difficult to Remove; Detachment of Device or Device Component

    IT WAS REPORTED THAT DURING AN ANGIOPLASTY PROCEDURE AT THE LOWER LEG, THE CATHETER OF THE PTA BALLOON ALLEGEDLY BROKE. THE PHYSICIAN WAS UNABLE TO SNARE OUT THE BROKEN PIECE FROM THE PATIENT. THE CURRENT PATIENT STATUS IS UNKNOWN.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 11775542 ↗

Other Catheter, percutaneous, cutting/scoring devices

All Catheter, percutaneous, cutting/scoring devices →

Sources and updates

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