RUSCH IPN042213Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04026704300884), received between Jul 27, 2023 and Jul 27, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Handling Problem” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 27, 2023Device Handling Problem; Device Handling Problem

  THE MEDWATCH REPORT STATES. "PATIENT WAS IN THE CARE OF EMS AND PRESENTING WITH SEIZURE LIKE ACTIVITY WHEN A ROBERTAZZI NASOPHARYNGEAL AIRWAY WAS PLACED. UPON ARRIVAL AT HOSPITAL PHYSICIAN BEGAN TO INITIATE INTUBATION AND NOTED THE NASOPHARYNGEAL AIRWAY HAD BECOME LODGED IN THE VOCAL CORDS." NO PATIENT HARM OR INJURY. "THE PHYSICIAN USED THE VIDEO LARYNGOSCOPY IN ORDER TO LOCATE THE NASAL PHARYNGEAL TRUMPET WHICH WAS PASSING THE CORDS. KELLY CLAMPS WERE USED TO REMOVE THE TRUMPET AND FACILITATE THE INTUBATION. NO ADDITIONAL OR EXCESSIVE FORCE WAS USED WHILE PLACING THE NPA. PATIENT BECAME COMBATIVE WHILE CARE WAS RENDERED. PATIENT WAS TRANSFERRED TO THE MICU AND SUCCESSFULLY EXTUBATES AND DISCHARGED ON (B)(6) 2023."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17407205 ↗