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VantageView™ VS100003Recalls & reported problems

St. Jude Medical, Inc. · System, 120V · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05415067010841), received between Jun 9, 2021 and Jun 9, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Display or Visual Feedback 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Display or Visual Feedback Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJun 9, 2021Display or Visual Feedback Problem; Display or Visual Feedback Problem

    DURING THE PROCEDURE WITH THE PATIENT WAS ON THE TABLE AND INTUBATED, THE SYSTEM LOST ALL VIDEO AFTER APPROXIMATELY 20-30 SECONDS. TROUBLESHOOTING DID NOT RESOLVE THE ISSUE AND THE PROCEDURE WAS CANCELLED WITH NO CONSEQUENCES TO THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11965832 ↗

Other DISPLAY, CATHODE-RAY TUBE, MEDICAL devices

All DISPLAY, CATHODE-RAY TUBE, MEDICAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.