Class II

Medical Device Recall: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S

Sarnova HC, Llc · February 12, 2024

Reason for Recall

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.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

550 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1308-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Sarnova HC, Llc Medical Device Recall: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S | SafeCheck