{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Republic",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89875",
      "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": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of Missouri.",
      "recall_number": "Z-1006-2022",
      "product_description": "Convenience kits containing regard IV Start Kits:  regard Clinical Packaging Solutions, Item Number: 830110002, IV01121B - IV Start Labor Birth.",
      "product_quantity": "950 convenience kits",
      "reason_for_recall": "A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation of test methods used in its manufacture.",
      "recall_initiation_date": "20220318",
      "center_classification_date": "20220426",
      "termination_date": "20240802",
      "report_date": "20220504",
      "code_info": "Lot numbers 89889, exp. 5/12/2022; 90446, exp. 5/12/2022; and 90641, exp. 5/12/2022.",
      "more_code_info": ""
    }
  ]
}