{
  "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": "Noblesville",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82036",
      "recalling_firm": "King Systems Corp. dba Ambu, Inc.",
      "address_1": "15011 Herriman Blvd",
      "address_2": "N/A",
      "postal_code": "46060-4253",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  CA, CT, FL, IA, IN, MD, MS, NC, PA, TX, and WI.",
      "recall_number": "Z-1681-2019",
      "product_description": "King LTS-D Kit Size 1, Model Number KLTSD431",
      "product_quantity": "270",
      "reason_for_recall": "Size 0 products were incorrectly packaged and labeled as a size 1 products.",
      "recall_initiation_date": "20190104",
      "center_classification_date": "20190529",
      "termination_date": "20200420",
      "report_date": "20190605",
      "code_info": "Lot code 1000147351"
    }
  ]
}