Vital Signs™ GK7FXXXXRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752125155), received between Jun 8, 2021 and Jun 8, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Suction Failure” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 8, 2021Suction Failure; Suction Failure

  THE CUSTOMER REPORTED 2 (TWO) DIFFERENT INCIDENTS FOR VENTED YANKAUER AND NON-VENTED YANKAUER. THE CUSTOMER REPORTED THAT THE LIMB-O¿ SINGLE LIMB ANESTHESIA BREATHING CIRCUIT EXPERIENCED A SUCTION PROBLEM AND SECRETION ISSUES WHILE SUCTIONING THE PATIENT. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11962945 ↗
• MalfunctionJun 8, 2021Suction Problem; Suction Problem

  THE CUSTOMER REPORTED 2 (TWO) DIFFERENT INCIDENTS FOR VENTED YANKAUER AND NON-VENTED YANKAUER. THE CUSTOMER REPORTED THAT THE LIMB-O¿ SINGLE LIMB ANESTHESIA BREATHING CIRCUIT EXPERIENCED A SUCTION PROBLEM AND SECRETION ISSUES WHILE SUCTIONING THE PATIENT. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11962944 ↗