{
  "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": "Ongoing",
      "city": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82787",
      "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": "NY, MN, NC, TX, GA, MO, PA, TN, NH, OH, CO",
      "recall_number": "Z-1838-2019",
      "product_description": "Cepheid Xpert C. difficile/Epi Control Panel",
      "product_quantity": "22 units",
      "reason_for_recall": "Product is labeled with expiration date of 2021-10-31, should be 2021-03-31.",
      "recall_initiation_date": "20190516",
      "center_classification_date": "20190618",
      "report_date": "20190626",
      "code_info": "UDI:  70845357041370, Lot Number 8200-26"
    }
  ]
}