Drug recall
Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Part Number: KLTSD404K Curaplex Ambu¿ King…
FDA recall event 85832 · Class II · Bound Tree Medical
Key facts
| Event ID | 85832 |
|---|---|
| Recall numbers | Z-2532-2020 |
| Recalling firm | Bound Tree Medical |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | May 14, 2020 |
| Report date | Jul 15, 2020 |
| Termination date | Dec 7, 2023 |
| City | Dublin |
| State | OH |
| Country | United States |
| FEI number | 3010792353 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: