RUSCH IPN040962Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704340894), received between Jul 25, 2022 and Jul 25, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inflation Problem” (1 report).

1 other recall cover devices cleared under the same FDA submission (K990619); they may or may not involve this specific model.

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.

• MalfunctionJul 25, 2022Inflation Problem; Inflation Problem

  IT WAS REPORTED THAT: "THE DOCTOR FOUND CUFF CANNOT BE INFLATED DURING CLINICAL SETTING BEFORE USING ON PATIENT. THEN STOPPED AND CHANGED NEW ONE. NO IMPACT ON PATIENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15092313 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K990619. One submission often covers many models, so check the product and lot details in each record.

• Z-1124-2015 · Dec 12, 2014 · Terminated
  RSCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be