Class II — Sarnova HC, Llc
| Recalling firm | Sarnova HC, LLC |
|---|---|
| Registered facility | TRI-ANIM HEALTH SERVICES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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. |
| 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. |
| Quantity | 1063 kits |
| Distribution | US Nationwide |
| Initiated | 2023-11-06 |
| Classified | 2024-01-12 |
| Recall number | Z-0720-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sarnova HC, Llc (Z-0720-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93665/
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