{
  "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": "Riviera Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83827",
      "recalling_firm": "Carroll-Baccari, Inc.",
      "address_1": "6625 White Dr",
      "address_2": "N/A",
      "postal_code": "33407-1209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US, Canada, Spain, England, and Australia",
      "recall_number": "Z-0368-2020",
      "product_description": "Lemon Prep:  MD0019T - 4 oz tubes  MD0019--SUP - Single Use Cups    Skin preparation used to enhance signal quality of patient recording electrodes (i.e. EKG, ECG, etc.)",
      "product_quantity": "24,979 units",
      "reason_for_recall": "Product has the potential to be contaminated with Burholderia cepacia.",
      "recall_initiation_date": "20190905",
      "center_classification_date": "20191113",
      "termination_date": "20211019",
      "report_date": "20191120",
      "code_info": "MD0019-T: 29824, 29901, 30006, 30145, 30236, 30352, 30675, 30729, 31138    MD0019-SUP:  29927, 30009, 30031, 30115, 30059, 30237, 30300, 30340, 30424, 30642, 30735, 31139"
    }
  ]
}