{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Republic",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90302",
      "recalling_firm": "ROi CPS LLC",
      "address_1": "3000 E Sawyer Rd",
      "address_2": "",
      "postal_code": "65738-2758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the state of FL.",
      "recall_number": "Z-1295-2022",
      "product_description": "regard Item Number: 800774001, CV00979A - CV Minor Kit, Sterile.",
      "product_quantity": "180 kits",
      "reason_for_recall": "A nonsterile component was packaged in a sterile convenience kit.",
      "recall_initiation_date": "20220520",
      "center_classification_date": "20220628",
      "termination_date": "20230502",
      "report_date": "20220706",
      "code_info": "Lot #91423, Exp. 02/08/2024, UDI (01)10194717101949(17)240208(10)91423.",
      "more_code_info": ""
    }
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}