{
  "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": "Republic",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90492",
      "recalling_firm": "ROi CPS LLC",
      "address_1": "3000 E Sawyer Rd",
      "address_2": "N/A",
      "postal_code": "65738-2758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distribution was made to MO.  There was no foreign/military/government distribution.",
      "recall_number": "Z-1408-2022",
      "product_description": "Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.",
      "product_quantity": "40 kits",
      "reason_for_recall": "Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.",
      "recall_initiation_date": "20220603",
      "center_classification_date": "20220719",
      "termination_date": "20230414",
      "report_date": "20220727",
      "code_info": "Lot #92605, exp. 8/31/2023, Item #830014016, UDI #10194717110156."
    }
  ]
}