# FDA recall Z-2532-2020

> **Bound Tree Medical** · Class II · device recall initiated 2020-05-14.

## 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

## Distribution

Nationwide Distribution

## Key facts

- **Recall number:** Z-2532-2020
- **Recalling firm:** Bound Tree Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-14
- **Report date:** 2020-07-15
- **Termination date:** 2023-12-07

- **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-2532-2020

## Citation

> AI Analytics. FDA recall Z-2532-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2532-2020. Source: US FDA. Licensed CC0.

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