{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
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      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
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      "address_1": "88 Inverness Cir E Unit A204",
      "address_2": "",
      "postal_code": "80112-5521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "USA Nationwide",
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      "product_quantity": "826 syringes",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20250521",
      "center_classification_date": "20250620",
      "report_date": "20250702",
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