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 | 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. |
| Product | Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S |
| Quantity | 540 kits |
| Distribution | US Nationwide distribution. |
| Initiated | 2024-02-12 |
| Classified | 2024-03-19 |
| Recall number | Z-1307-2024 |
| 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-1307-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94116/
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