Sarnova recalls Curaplex Nasal Intubation Kits with 7mm endotracheal tubes due to incompatible tube holder affecting nasal intubation safety. Affected kits include specific lot numbers and item numbers.
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.
Sarnova is recalling Curaplex Nasal Intubation Kits with 7mm endotracheal tubes because the included tube holder isn't compatible with nasal intubation procedures. This could leave medical professionals without a way to secure the tube during emergency airway management. Read more at govinfonow.com/recall/56167-sarnova-curaplex-nasal-intubation-kit-incompatible-tube-holder-risk.
“Sarnova Curaplex Nasal Intubation Kit: Incompatible Tube Holder Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56167-sarnova-curaplex-nasal-intubation-kit-incompatible-tube-holder-risk. Based on FDA recall #Z-1308-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1308-2024%22&limit=1).
The FDA announced on Feb. 12, 2024, that Sarnova HC, Llc is recalling Curaplex Nasal Intubation Kits because the included endotracheal tube holder is incompatible with nasal intubation procedures. This defect leaves practitioners without the means to secure the inserted tube.
Lot Numbers: ASM0038078, ASM0038130, ASM0038284, ASM0038395
The hazard
The endotracheal tube holder included in certain kits is not compatible with a nasal intubation procedure. This incompatibility leaves practitioners without the necessary means to secure the inserted endotracheal tube.
Context
GovInfoNow's records show Sarnova HC, Llc has one other recall on record since Nov. 6, 2023: a Curaplex Field Cric Kit recalled for an incompatible endotracheal tube holder. Other recent recalls of similar products include Medline Intubation Tray Recall (Dec. 24, 2025), Elekta Fletcher CT/MR Shielded Applicator Set Recall (April 3, 2026), and Elekta Geneva Brachytherapy Applicator Recall (April 3, 2026).
How to tell if you have this one
Check for item number 023070S or UDI/GTIN 00815277020015 (each) or 00810071639647 (case). Affected kits have lot numbers ASM0038078, ASM0038130, ASM0038284, or ASM0038395.
Brand
Sarnova
Product
Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution.
Recall number
Product, codes & lots
Quantity
Z-1307-2024
Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S; UDI/GTIN: 00815277020008 each, 00810071639630 case Lot Numbers: ASM0038077 ASM0038129 ASM0038334 ASM0038598
540 kits
Z-1308-2024
Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S; UDI/GTIN: 00815277020015 each, 00810071639647 case Lot Numbers: ASM0038078 ASM0038130 ASM0038284 ASM0038395
550 units
Based on the official FDA remedy
What to do — step by step
Check Kit Details
Verify the item number, UDI/GTIN, and lot numbers listed in the recall notice to confirm if your kit is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 44 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1308-2024 (February 12, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1308-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.