FDA Device Intelligence
Home › Device types › EPE

Brush, Cleaning, Tracheal Tube

FDA product code EPE · Class 1 · Anesthesiology

162
Registered devices
6
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.