{
  "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": "Riviera Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84587",
      "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": "Press Release",
      "distribution_pattern": "Nationwide, Canada, UK, Spain, Australia",
      "recall_number": "Z-1550-2020",
      "product_description": "MVAP MEDICAL SUPPLIES INC, Mavidon CardioPrep Single, 24 use cups, Re order #  MCP-24",
      "product_quantity": "240 units",
      "reason_for_recall": "Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug Administration inspection on October 15, 2019 were tested and found to be contaminated with Burkholderia cepacia. Mavidon is recalling all products manufactured at their facility.",
      "recall_initiation_date": "20191223",
      "center_classification_date": "20200320",
      "termination_date": "20210928",
      "report_date": "20200401",
      "code_info": "All Lots",
      "more_code_info": ""
    }
  ]
}