{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "192230",
      "product_res_number": "Z-0784-2022",
      "event_date_initiated": "2022-02-25",
      "event_date_created": "2022-03-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2024-01-16",
      "res_event_number": "89694",
      "product_code": "OHQ",
      "product_description": "Mycoplasma genitalium Control Panel (Inactivated Pellet)",
      "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)",
      "firm_fei_number": "2150138",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "city": "Saint Cloud",
      "state": "MN",
      "postal_code": "56303-4440",
      "additional_info_contact": "Becky Neu\n320-229-7073",
      "reason_for_recall": "Distributed product did not undergo proper release testing.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "All consignees were contacted beginning 02/25/2022 via email.  Consignees should read the recall instructions and determine if the product can be used or discarded, depending on user's lab procedures.  A response form should be completed and returned to recall@microbiologics.com.",
      "product_quantity": "80 units",
      "distribution_pattern": "Distribution in US: AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY, PA, TX, UT, WA\n\nOUS distribution to Belgium, Finland, France, Germany, Ireland, Sweden, United Kingdom, and Vietnam",
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        "device_name": "Multi-Analyte Controls Unassayed",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.1660",
        "device_class": "1"
      }
    }
  ]
}