{
  "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": "Framingham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63305",
      "recalling_firm": "New England Compounding Center",
      "address_1": "697 Waverly St",
      "address_2": "N/A",
      "postal_code": "01702-8589",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-119-2013",
      "product_description": "Isovue 200 mg/mL PF and 300 mg/mL PF, Vials, manufactured by New England Compounding Center, Framingham, MA",
      "product_quantity": "7055 vials",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20120926",
      "center_classification_date": "20121231",
      "termination_date": "20161007",
      "report_date": "20130109",
      "code_info": "All lot codes"
    }
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}