# FDA recall Z-1307-2024

> **Sarnova HC, Llc** · Class II · device recall initiated 2024-02-12.

## Product

Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency.  Item Number: 023060S

## Reason for recall

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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1307-2024
- **Recalling firm:** Sarnova HC, Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-12
- **Report date:** 2024-03-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dublin, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1307-2024

## Citation

> AI Analytics. FDA recall Z-1307-2024. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1307-2024. Source: US FDA. Licensed CC0.

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