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# Teleflex Recalls Endotracheal Tubes
- URL: https://www.fdaweb.com/teleflex-recalls-endotracheal-tubes/
- Published: 2023-06-30T12:00:00.000Z
- Updated: 2026-09-14T18:42:26.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5154809

Teleflex has recalled (Class 1) its Slick Set Uncuffed Endotracheal Tube and Stylet Set (oral/nasal) due to reports about the 15mm connector disconnecting from the endotracheal tube. The company recently sent an “urgent medical device recall” notice to users that advised to stop using affected products and immediately quarantine them, according to a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=200866&ref=fdaweb.com). The cause of the device malfunction is under investigation by the firm, it says.