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# Medline Recalls Endotracheal Tube
- URL: https://www.fdaweb.com/medline-recalls-endotracheal-tube/
- Published: 2024-05-29T12:00:00.000Z
- Updated: 2026-09-14T14:31:59.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157075

Medline Industries has recalled (Class 1) its Medline Sub-G Endotracheal Tube with Subglottic Suctioning after complaints were received about the device’s inflation tube detaching from the main tube. If a detachment occurs, this could result in potential moisture buildup, loss of pressure, or inability to inflate, [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=206447&ref=fdaweb.com) says. There were also reports the suction pump is difficult to connect or detaches during use. The issue is under investigation by Medline.