CARDINAL HEALTH K86VRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885380028710), received between May 10, 2023 and May 10, 2023 — classified as 1 malfunction.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 10, 2023Suction Failure; Suction Failure

  THE CUSTOMER REPORTED THAT ON (B)(6) 2023 THE PATIENT BECAME LESS RESPONSIVE. RRT WAS CALLED AND SUCTION SET UP WAS COMPLETED AND ACCURATE, BUT NO SUCTION WAS ACHIEVED THROUGH THE YANKAUER. THE REGULATOR WAS SWITCHED BUT AGAIN NO SUCTION. CRASH CART SUCTION WAS THEN SET UP BY NURSING WITH THE SAME RESULT. RT NOW PRESENT AND ADVISES TO TRY A NEW YANKAUER WHICH WAS EFFECTIVE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16901760 ↗