Halyard 45835Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10680651458350), received between Feb 1, 2019 and Feb 1, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Disconnection” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 1, 2019Disconnection; Disconnection

  AVANOS MEDICAL RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENTS, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THE SAME PATIENT. THIS IS THE FIRST OF TWO REPORTS. REFER TO 3011270181-2019-00003 FOR THE SECOND PATIENT. IT WAS REPORTED THAT AN ATTEMPT WAS MADE TO INSERT A CORGRIP DEVICE INTO A PATIENT. IN DOING SO, THE MAGNET ON THE TAPE SIDE BECAME DISCONNECTED FROM THE TAPE. NO PATIENT INJURY NOTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8296113 ↗
• MalfunctionFeb 1, 2019Disconnection; Disconnection

  AVANOS MEDICAL RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENTS, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING A SINGLE PATIENT. THIS IS THE SECOND OF TWO REPORTS. REFER TO 3011270181-2019-00002 FOR THE SECOND PATIENT. IT WAS REPORTED THAT AN ATTEMPT WAS MADE TO INSERT A CORGRIP DEVICE INTO A PATIENT. IN DOING SO, THE MAGNET REMAINED IN THE PATIENT'S NOSE BUT WAS ABLE TO BE RETRIEVED BY REINSERTING THE YELLOW PROBE AND RECONNECTING THE MAGNET. NO PATIENT INJURY NOTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8296110 ↗