{
  "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": "2026-03-18",
    "results": {
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      "status": "Terminated",
      "city": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90150",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "address_2": "",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed US Nationwide to IA, TN and internationally to Mexico, Colombia, France, South Africa, United Kingdom.",
      "recall_number": "Z-1125-2022",
      "product_description": "KWIK-STIK\" plus: Clostridium perfringens",
      "product_quantity": "8 units",
      "reason_for_recall": "Labeling error.",
      "recall_initiation_date": "20220506",
      "center_classification_date": "20220523",
      "termination_date": "20240116",
      "report_date": "20220601",
      "code_info": "catalog number: 0801P; lot number: 801-44-4; expiration date: 05/31/2023; UDI: 20845357019374",
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}