Device recall
Z-1308-2024: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal…
FDA device recall · Class II · Sarnova HC, Llc
Key facts
| Recall number (Z-number) | Z-1308-2024 |
|---|---|
| Recall event | 94116 |
| Product | Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S |
| Product code | LNZ |
| Recalling firm | Sarnova HC, Llc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3014680755 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database