{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89694",
      "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": "Distribution in US: AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY, PA, TX, UT, WA    OUS distribution to Belgium, Finland, France, Germany, Ireland, Sweden, United Kingdom, and Vietnam",
      "recall_number": "Z-0784-2022",
      "product_description": "Mycoplasma genitalium Control Panel (Inactivated Pellet)",
      "product_quantity": "80 units",
      "reason_for_recall": "Distributed product did not undergo proper release testing.",
      "recall_initiation_date": "20220225",
      "center_classification_date": "20220314",
      "termination_date": "20240116",
      "report_date": "20220323",
      "code_info": "Catalog 8240, Lots: 8240-08, 8240-09, 8240-10, 8240-11, 8240-12, 8240-13, 8240-14, 8240-15, 8240-16 (UDI: 70845357043053)"
    }
  ]
}