{
  "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": "2026-04-22",
    "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": "89479",
      "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 Nationwide and the countries of Canada, South Africa, France, Netherlands, Mauritius, China.",
      "recall_number": "Z-0641-2022",
      "product_description": "KWIK-STIK(TM), Quality control kit for culture media, sold as:     KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)",
      "product_quantity": "10 units",
      "reason_for_recall": "Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating this is a labeling error and the organism is the correct organism.",
      "recall_initiation_date": "20130325",
      "center_classification_date": "20220214",
      "termination_date": "20220422",
      "report_date": "20220223",
      "code_info": "Catalog Number 01023P, UDI: 20845357029502, Lot Number (Expiration Date): 1023-05-7 (04/30/2014)"
    }
  ]
}