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Sarnova HC, Llc recalls Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emerge
Recalled March 27, 2024 · FDA recall Z-1308-2024 · Sarnova HC
Hazard
Endotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube. · FDA Class II
Units
550 units
Sold at
US Nationwide distribution.
Description
Endotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube.
Product
Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S
Manufacturer(s)
Sarnova HC, Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →