Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Recalled by Bound Tree Medical Due to Kit contained an incorrect catheter-tip syringe not compatible...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bound Tree Medical directly.
Affected 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 components necessary to successfully obtain an open patient airway with an Ambu¿ King LTS-D" Supraglottic Airway.
Quantity: 167 kits
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bound Tree Medical
Bound Tree Medical has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report