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Device, Fixation, Tracheal Tube

FDA product code CBH · Class 1 · Anesthesiology

400
Registered devices
822
Adverse events
12
Recalls
47
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbo
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbo
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbo
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbo
2017-03-24Dale Medical Products, Inc.ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.
2017-03-24Dale Medical Products, Inc.ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.

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