Bound Tree Medical recalls Curaplex Ambu King LTS-D Supraglottic Airway Kits with part number KLTSD404K due to incorrect catheter tip syringe that may prevent proper airway sealing during medical procedures.
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
Bound Tree Medical is recalling Curaplex Ambu King LTS-D Supraglottic Airway Kits with part number KLTSD404K because the included catheter-tip syringe is incompatible with the airway's luer lock connector. This could prevent the kit from creating a secure airway seal in patients, potentially causing breathing issues during medical procedures.
The kit includes a catheter-tip syringe that doesn't match the luer lock connector on the airway. This incompatibility may prevent the airway from inflating properly, which is necessary to create a secure seal in the patient's airway. If the seal fails, the patient could have breathing difficulties during medical procedures.
Healthcare professionals using the Curaplex Ambu King LTS-D Supraglottic Airway Kit with part number KLTSD404K are most at risk. Patients receiving this kit during medical procedures could experience breathing difficulties if the airway seal fails.
Check for the part number KLTSD404K on the kit. The product was sold with lot number ASM0025699. This specific kit is used for medical airway procedures.
Verify if the kit includes a catheter-tip syringe that is compatible with the luer lock connector of the airway.
The kit contains an incorrect catheter-tip syringe that may not be compatible with the luer lock connector of the airway, potentially preventing proper airway sealing during medical procedures.
Look for part number KLTSD404K on the kit.
The official recall notice does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Bound Tree Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2532-2020 — Bound Tree Medical Bound Tree Medical Hello, I own a Bound Tree Medical that is covered by recall Z-2532-2020 from Bound Tree Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
