Vital Signs™ B1734XX4Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752124059), received between Nov 24, 2021 and Nov 24, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Blocked Connection” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryNov 24, 2021Blocked Connection; Blocked Connection

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE B1734XX4-VITAL SIGNS® PEDIATRIC ANESTHESIA BREATHING CIRCUIT IS OCCLUDED WHILE CONNECTED TO THE PATIENT. ANOTHER NEW SAMPLE LINE WAS ADDED AND THE "SAMPLE LINE" ERROR WENT AWAY AND THE PATIENTS CO2 READING CAME ACROSS THE MONITOR SCREEN. AT THIS TIME, THE CUSTOMER HAS NOT PROVIDED ANY INFORMATION REGARDING PATIENT HARM OR INJURY ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12870883 ↗