Vital Signs™ 73319-HELRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752117181), received between Jan 19, 2024 and Jan 19, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Partial 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. How this data works · Data updated Oct 13, 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.

• MalfunctionJan 19, 2024Partial Blockage; Partial Blockage

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE 73319-HEL - GAS SAMPLING LINE, 10FT, M/M WAS PARTIALLY OCCLUDED, CAUSING THE ANESTHESIA MACHINE TO GO INTO A CHECK DEFEND ALARM STATUS. THOUGH THERE WERE HALF-HOUR DELAYS DURING THE SURGERY, THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18544347 ↗