{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Dallas",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72455",
      "recalling_firm": "Downing Labs, LLC",
      "address_1": "4001 McEwen Rd Suite 110",
      "address_2": "N/A",
      "postal_code": "75244-5020",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide in the US; Australia, Brazil, Bahamas, Switzerland, France, Colombia, Hong Kong, Indonesia, India, Japan, Malaysia, New Zealand, Phillippines, Singapore, Thailand, Trinidad and Tobago, Taiwan",
      "recall_number": "D-0347-2016",
      "product_description": "Vitamin D3 Injectable, 10,000 U/mL, 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435",
      "product_quantity": "27 vials",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20151016",
      "center_classification_date": "20151118",
      "termination_date": "20160922",
      "report_date": "20151125",
      "code_info": "All lots"
    }
  ]
}