{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85832",
      "recalling_firm": "Bound Tree Medical",
      "address_1": "5000 Tuttle Crossing Blvd",
      "address_2": "",
      "postal_code": "43016-1534",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-2532-2020",
      "product_description": "Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube \t  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_quantity": "167 kits",
      "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",
      "recall_initiation_date": "20200514",
      "center_classification_date": "20200707",
      "termination_date": "20231207",
      "report_date": "20200715",
      "code_info": "Lot Number: ASM0025699",
      "more_code_info": ""
    }
  ]
}