Halyard 13224Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651132243), received between Jul 20, 2017 and Jul 20, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment Of Device Component” (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 16, 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.

• MalfunctionJul 20, 2017Detachment Of Device Component; Detachment Of Device Component

  IT WAS REPORTED THAT THE ENDOTRACHEAL TUBE ADAPTER DISCONNECTS TOO EASILY, RESULTING IN A DISCONNECTION OF THE PATIENT FROM THE VENTILATOR. THIS HAPPENS FREQUENTLY AFTER USING AN AMBU BAG ON THE ADAPTER. PER ADDITIONAL INFORMATION WAS RECEIVED ON 29-JUN-2017, THERE WAS NO PATIENT INJURY AND NO MEDICAL INTERVENTION. NO ADDITIONAL INFORMATION WAS PROVIDED AT THIS TIME.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6728721 ↗