Home / Recalls / Medical Devices
TELEFLEX LLC recalls Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585
Recalled July 5, 2023 · FDA recall Z-1852-2023 · TELEFLEX
Hazard
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. · FDA Class I
Units
56640 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
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585
Manufacturer(s)
TELEFLEX LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →