Device recall
Z-2532-2020: Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Part Number…
FDA device recall · Class II · Bound Tree Medical
Key facts
| Recall number (Z-number) | Z-2532-2020 |
|---|---|
| Recall event | 85832 |
| Product | Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Part Number: KLTSD404K Curaplex Ambu King LTS-D" Supraglottic Airway Kit with ET Tube (hereafter the Kit which contains all of the components necessary to successfully obtain an open patient airway with an Ambu King LTS-D" Supraglottic… |
| Product code | CAE |
| Recalling firm | Bound Tree Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 7, 2023 |
| FEI number | 3010792353 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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