Vital Signs™ A1UXOXXXRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752119215), received between Sep 26, 2023 and Sep 26, 2023 — classified as 1 malfunction.

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

• MalfunctionSep 26, 2023Complete Blockage; Complete Blockage

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE Y-PIECE OF A1UXOXXX ANES CIRCUIT, ADULT, 108 IN EXP, 2L BAG IS BLOCKED. VENTILATION FOR THE PATIENT WAS NOT POSSIBLE. THE PATIENT WAS INITIALLY SPONTANEOUSLY BREATHING AND WAS ALSO KEPT THAT WAY DURING THE SEARCH FOR THE CAUSE.AFTER RULING OUT ANY PROBLEM ON THE PATIENT'S SIDE MANUAL VENTILATION WAS PERFORMED ON THE PATIENT VIA ANESTHESIA BAG.ONLY AFTER CHANGING THE BREATHING CIRCUIT ON THE PRIMUS THAT THE VENTILATION WORKED PROPERLY. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17819223 ↗