AVANOS 20-7432AIV2Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00350770457604), received between Oct 12, 2022 and Oct 25, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Twisted/Bent” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionOct 25, 2023

  AVANOS NASOGASTRIC/NASO-INTESTINAL FEEDING TUBE WAS LEAKING NUTRITIONAL CONTENT WHILE IN THE PATIENT. NURSE WIPED LIQUID AWAY, BUT TUBING CONTINUED TO LEAK. THE FEEDING TUBE WAS REMOVED AND EXAMINED; THERE WAS A SLIT IN THE TUBING. NEW FEEDING TUBE INSERTED, NO KNOWN PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18002614 ↗
• MalfunctionOct 12, 2022Material Twisted/Bent

  UPPER 50¿S MALE IN LONG-TERM ACUTE CARE. CORFLO FEEDING TUBE, 12 FR, INSERTED WITHOUT DIFFICULTY. 2 X-RAYS CONFIRMED THAT THE TIP WAS KINKED AT A RIGHT ANGLE. FEEDING TUBE REMOVED AND ANOTHER ONE INSERTED WITHOUT DIFFICULTY. NO KNOWN HARM TO PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15592605 ↗