Curaplex Field Cric Kit with ET Tube — Class II medical device recall Z-0720-2024
Ongoing recall by Sarnova HC, Llc, reported 2024-01-24, distributed nationwide. It was determined that the Endotracheal Tube Holder included in certain kits is not compatible with a cricothy
| Recall number | Z-0720-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sarnova HC, Llc, Dublin, OH, United States |
| Recall initiated | 2023-11-06 |
| Classified | 2024-01-12 |
| Reported by FDA | 2024-01-24 |
| Distributed | Nationwide (US) |
| Quantity | 1,063 kits |
| Lot numbers | ASM0037579, ASM0037631, ASM0037905, ASM0038197 |
| Model numbers | 36611 |
Product
Curaplex Field Cric Kit with ET Tube, Item Number 36611. The kit provides healthcare professionals with an assortment of supplies to perform a cricothyrotomy.
Reason for recall
It was determined that the Endotracheal Tube Holder included in certain kits is not compatible with a cricothyrotomy procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0720-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.