PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: March 27, 2024 Initiated: February 12, 2024 #Z-1308-2024

Product Description

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

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.

Details

Recalling Firm
Sarnova HC, Llc
Units Affected
550 units
Distribution
US Nationwide distribution.
Location
Dublin, OH

Frequently Asked Questions

What product was recalled?
Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S. Recalled by Sarnova HC, Llc. Units affected: 550 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 27, 2024. Severity: Moderate. Recall number: Z-1308-2024.