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TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
Recalled July 5, 2023 · FDA recall Z-1942-2023 · TELEFLEX
Hazard
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. · FDA Class I
Units
23395 units
Sold at
US Nationwide distribution including Puerto Rico.
Description
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
Manufacturer(s)
TELEFLEX LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →