Bound Tree Medical: Medical Device Recall in 2020 - (Recall #: Z-2532-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: May 14, 2020

Date Posted: July 15, 2020

Recall Number: Z-2532-2020

Event ID: 85832

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

Status: Terminated

Product Quantity: 167 kits

Code Information:

Lot Number: ASM0025699

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated