{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93267",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "address_2": "N/A",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Italy, France, Turkey, Peru, Mexico.",
      "recall_number": "Z-0307-2024",
      "product_description": "KWIKSTIK, P. venetum, Catalog numbers:  a) 0794P (2-pack),  b) 0794K (6-pack)",
      "product_quantity": "13 units",
      "reason_for_recall": "A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.",
      "recall_initiation_date": "20231018",
      "center_classification_date": "20231115",
      "report_date": "20231122",
      "code_info": "a) UDI/DI 20845357019169, Lot Numbers:  794-142-2, 794-142-4 b) UDI/DI 30845357019173, Lot Numbers:  794-142-3"
    }
  ]
}