Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Part… — Class II medical device recall Z-2532-2020
Terminated recall by Bound Tree Medical, reported 2020-07-15, distributed nationwide. Kit contained an incorrect catheter-tip syringe not compatible with the luer lock connector of the included ai
| Recall number | Z-2532-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bound Tree Medical, Dublin, OH, United States |
| Recall initiated | 2020-05-14 |
| Classified | 2020-07-07 |
| Reported by FDA | 2020-07-15 |
| Terminated | 2023-12-07 |
| Distributed | Nationwide (US) |
| Quantity | 167 kits |
| Reason classes | packaging |
| Lot numbers | ASM0025699 |
| Model numbers | KLTSD404K |
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 Airway.
Reason for recall
Kit contained an incorrect catheter-tip syringe not compatible with the luer lock connector of the included airway. As a result, may be unable to inflate the balloons of the supraglottic airway to create a secure seal in the patient s airway as intended by the kit
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2532-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.