HUDSON RCI IPN916671Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704717757), received between Jul 25, 2023 and Jul 25, 2023 — classified as 1 malfunction.

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.

• MalfunctionJul 25, 2023No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT WHILE IN USE, THE PATIENT "CHEWED OFF THE ENDS OF THE HME. LAST NIGHT HE ALMOST SWALLOWED THE ENDS TWICE. HE IS CONSTANTLY CHEWING OFF THE ENDS OF THE HME, WHICH, UNFORTUNATELY, COME OFF VERY EASILY. THIS EPISODE HAPPENED AT NIGHT, AND LUCKILY THE FATHER WAS ABLE TO RETRIEVE THE OBJECT BEFORE IT DID ANY DAMAGE. MY CLIENT DID NOT REQUIRE ANY MEDICAL INTERVENTION AND HAS DONE VERY WELL SINCE". NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17389507 ↗