{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Charles",
      "state": "MO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72619",
      "recalling_firm": "BC Group International Inc",
      "address_1": "3081 Elm Point Industrial Dr",
      "address_2": "N/A",
      "postal_code": "63301-4333",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution in the states of South Carolina, Florida, and Canada.",
      "recall_number": "Z-0457-2016",
      "product_description": "DA-2006P - Defibrillator / Pacer Analyzer;    Product Usage:  Intended to measure the output of a defibrillator or transcutaneous pacemaker.",
      "product_quantity": "5 units",
      "reason_for_recall": "Device is not functioning as intended:  Two wires running to the ECG distribution circuit board are reversed resulting in inverted waveforms.",
      "recall_initiation_date": "20151028",
      "center_classification_date": "20151221",
      "termination_date": "20170215",
      "report_date": "20151230",
      "code_info": "SN:  73962222, 73962223, 73962224, 73962225, and 73962226"
    }
  ]
}