{
  "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": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89379",
      "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": "Letter",
      "distribution_pattern": "Worldwide distribution - US distribution in the states of GA, MS, MT, NC, NM, NV, TN, TX, WA, WI and the countries of  Brazil, Canada, China, Colombia, Dominican Republic, France, India, Ireland, Japan, Mexico, Oman, Philippines, Romania, South Africa, Turkey, United Arab Emirates.",
      "recall_number": "Z-0543-2022",
      "product_description": "KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P.  Packaged 2 units per pack.  IVD controls.",
      "product_quantity": "65 packs (130 units)",
      "reason_for_recall": "Potential that products packaged for lot 726-57-10 were packaged in pouches labeled as 323-108-7.",
      "recall_initiation_date": "20210224",
      "center_classification_date": "20220128",
      "termination_date": "20220711",
      "report_date": "20220209",
      "code_info": "Catalog Number: 0726P,  Lot Number: 726-57-10,  UDI: 20845357017486"
    }
  ]
}