FDA Device Intelligence
HomeDevice types › BTR

Tube, Tracheal (W/Wo Connector)

FDA product code BTR · Class 2 · Anesthesiology

4,433
Registered devices
19,094
Adverse events
226
Recalls
241
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-02-13Smiths Medical ASD, Inc.Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, unde
2024-02-26MEDLINE INDUSTRIES, LP - NorthfieldComplaints have been received that the device inflation tube detached and/or tore from the main tube, resulting in potential moisture buildup, loss of pressure,
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
2023-05-25TELEFLEX LLCReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.