Halyard 45755Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651457551), received between Apr 9, 2020 and Apr 9, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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.

• MalfunctionApr 9, 2020Difficult to Remove; Difficult to Remove

  A REPORT WAS RECEIVED VIA FDA MEDWATCH / FDA USER FACILITY REPORT # (B)(4) AND THE FOLLOWING INFORMATION WAS PROVIDED: NURSE [W]AS ATTEMPTING TO REMOVE WEIGHTED NASOGASTRIC TUBE FROM PATIENT TUBE [W]OULD NOT COME OUT EAR/NOSE/THROAT DOCTOR CONSULTED. TUBE PULLED TO STOPPAGE POINT THROUGH NOSE. PHYSICIAN THEN CUT TUBE AND REMOVED BOTTOM HALF THROUGH MOUTH. BOTTOM HALF OF TUBE WAS IN A KNOT." NO INJURY REPORTED. EVENT DATE ENTERED MEDWATCH FORM AS (B)(6) 2020.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9946810 ↗