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TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
Recalled July 5, 2023 · FDA recall Z-1888-2023 · TELEFLEX
Hazard
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. · FDA Class I
Units
860472 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
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
Manufacturer(s)
TELEFLEX LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →