{
  "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": "2026-07-08",
    "results": {
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    {
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      "city": "W Lafayette",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95149",
      "recalling_firm": "Cook Biotech, Inc.",
      "address_1": "1425 Innovation Pl",
      "address_2": "",
      "postal_code": "47906-1000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Canada,  China, Finland, France, Germany, Ireland, Luxembourg, Netherlands, New Zealand,  Norway, South Africa, United Kingdom.",
      "recall_number": "Z-3257-2024",
      "product_description": "Biodesign Fistula Plug C-FPS-0.7-2 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas.    Order Number (GPN): G46373",
      "product_quantity": "130 units",
      "reason_for_recall": "Products expire prior to the expiration date printed on the product labeling",
      "recall_initiation_date": "20240807",
      "center_classification_date": "20240925",
      "report_date": "20241002",
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