RUSCH IPN040719Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

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

6 other recalls cover devices cleared under the same FDA submission (K931165); 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-1923-2023 · Root cause: Under Investigation by firm · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K931165. One submission often covers many models, so check the product and lot details in each record.

• Z-1872-2023 · May 25, 2023 · Open, Classified
  Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045
• Z-1873-2023 · May 25, 2023 · Open, Classified
  Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050
• Z-1871-2023 · May 25, 2023 · Open, Classified
  Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040
• Z-1924-2023 · May 25, 2023 · Open, Classified
  Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065
• Z-1870-2023 · May 25, 2023 · Open, Classified
  Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
• Z-1922-2023 · May 25, 2023 · Open, Classified
  Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055