Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To… recallZ-1307-2024 · Sarnova HC, Llc · initiated Feb 12, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Sarnova HC, Llc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was 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.
FDA root cause category: Component design/selection
What the company is doing
Bound Tree issued URGENT NOTICE OF RECALL letters on February 12, 2024 via USPS Letter to Medical Inventory Controls/Supplies Coordinator/Buyer. Letter states reason for recall, health risk and actin to take: Should you determine your inventory contains product covered by this recall, please immediately quarantine your affected product and contact Bound Tree Medical Customer Care at 800.533.0523 to arrange for a return of the product in exchange for a credit
Recall details
- Recall number
- Z-1307-2024
- Status
- Open, Classified
- Initiated by the company
- Feb 12, 2024
- Posted by the FDA
- Mar 19, 2024
- Recalling firm
- Sarnova HC, Llc
- Quantity
- 540 kits
- Product code
- LNZ
- Distribution
- US Nationwide distribution.
Product description
Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S
Code information (models, lots, serial numbers)
UDI/GTIN: 00815277020008 each, 00810071639630 case Lot Numbers: ASM0038077 ASM0038129 ASM0038334 ASM0038598
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Curaplex 023060SBound Tree Medical, LLC · Changer, tube, endotracheal1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 94116).
- Z-1308-2024 · Open, ClassifiedCuraplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
How recalls are matched to devices · Editorial policy · Report an error on this page