Vital Signs™ A8UB20X4Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752121171), received between Aug 9, 2022 and Aug 9, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Disconnection” (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.

• InjuryAug 9, 2022Disconnection; Disconnection

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE ANES CIRCUIT, ADULT, 108 IN EXP, 3L BAG DISCONNECT FROM THE WYE WHILE CONNECTED TO A PATIENT. THE CIRCUIT WAS RECONNECTED TO THE WYE DURING THE PATIENT'S PROCEDURE AND NO FURTHER ACTIONS WERE REQUIRED. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15196260 ↗