RUSCH IPN041448Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 14026704341228), received between Aug 13, 2025 and Aug 13, 2025 — classified as 11 malfunctions.

The most frequently reported specific device problem is “Gas/Air Leak” (11 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. May 25, 2023Open, Classified

   Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

   Z-1956-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22792284 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22792255 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22792028 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22792023 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22792007 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22791993 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22791981 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT "THE CUFF WILL NOT HOLD AIR, PRIOR TO USE. NO PATIENT INVOLVED.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22791902 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT: "THE CUFF WILL NOT HOLD AIR AND IS DEFLATING WHILE INSIDE THE PATIENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22791554 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT: "THE CUFF WILL NOT HOLD AIR AND IS DEFLATING WHILE INSIDE THE PATIENT.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22791552 ↗
• MalfunctionAug 13, 2025Gas/Air Leak; Gas/Air Leak

  IT WAS REPORTED THAT: "THE CUFF WILL NOT HOLD AIR AND IS DEFLATING WHILE INSIDE THE PATIENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22791539 ↗