RUSCH IPN040776Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704340801), received between Jun 1, 2023 and Jun 1, 2023 — classified as 1 malfunction.

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

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

23 other recalls cover devices cleared under the same FDA submission (K961840); 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. How this data works · Data updated Oct 13, 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-1875-2023 · Root cause: Under Investigation by firm · FDA record ↗

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.

• MalfunctionJun 1, 2023Failure to Disconnect; Compatibility Problem; Failure to Disconnect; Compatibility Problem

  IT WAS REPORTED THAT "WE WERE UNABLE TO REMOVE THE HUB FROM THE ENDOTRACHEAL TUBE". NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE". ADDITIONAL INFORMATION RECEIVED STATES THAT THE INDICATION FOR USE OF THE ETT WAS THAT THE PATIENT REQUIRED MECHANICAL VENTILATION WITH MEDICAL MANAGEMENT IN CRITICAL CARE. THE ISSUE WAS RESOLVED BY CUTTING THE ETT TO REMOVE THE ADAPTOR. THE PATIENT DID NOT REQUIRE REINTUBATION. THE PATIENT DID NOT EXPERIENCE ANY OXYGEN DESATURATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17040330 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K961840. One submission often covers many models, so check the product and lot details in each record.

• Z-1937-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
• Z-1926-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030
• Z-1929-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380045
• Z-1930-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050
• Z-1932-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060
• Z-1874-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030
• Z-1925-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380025
• Z-1928-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380040
• Z-1936-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
• Z-1856-2023 · May 25, 2023 · Open, Classified
  Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535
• Z-1927-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035
• Z-1859-2023 · May 25, 2023 · Open, Classified
  Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506550
• Z-1855-2023 · May 25, 2023 · Open, Classified
  Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530
• Z-1876-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
• Z-1933-2023 · May 25, 2023 · Open, Classified
  Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380065

…and 8 more.