Vital Signs™ B1513XXXRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752123816), received between Mar 26, 2021 and Oct 26, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Disconnection” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 26, 2021Disconnection; Disconnection

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE VITAL SIGNS PEDIATRIC ANESTHESIA BREATHING CIRCUIT ARE COMING APART AND DETACHING WITH SMALL EFFORT AT THE Y CONNECTOR. THERE WAS NO INFORMATION ON PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12701525 ↗
• MalfunctionMar 26, 2021Disconnection; Disconnection

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE VITAL SIGNS PEDIATRIC ANESTHESIA BREATHING CIRCUIT ARE COMING APART AND DETACHING WITH SMALL EFFORT AT THE Y CONNECTOR. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11577325 ↗