FDADecember 8, 2022device
Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal; b. Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff; c. RUSCHELIT Super Safety Clear Tracheal Tube, oral/nasal, Murphy. Intended for patients requiring endotracheal...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Potential for pilot balloon non-inflation or cuff non-deflation.
What to do
FDA enforcement status: Ongoing
Brands named
teleflex
UPCs
4026704547579402670454759340267045476304026704547647402670454765414026704341389140267043413961402670434140214026704341419140267043414261402670434143314026704341440
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820552023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820502023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120800952023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120800552023-05-25
- FDARUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 1124800302023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120801002023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820902023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820602023-05-25
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