Vital Signs™ B1754XT4Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752124103), received between Jan 30, 2023 and Jan 30, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Connection 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. 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.

• InjuryJan 30, 2023Connection Problem; Connection Problem

  THE CUSTOMER REPORTED TO VYAIRE MEDICAL THAT CIRCUIT HAS A LOOSE CONNECTION BETWEEN THE ELBOW AND CAME APART DURING SURGERY. THE SIZE OF THE CIRCUIT IS SMALLER FROM THAN IT SHOULD BE. ANESTHESIA DISCONNECTION WAS QUICKLY RECOGNIZED AND THE CIRCUIT WAS RECONNECTED. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16268676 ↗