{
  "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 I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93653",
      "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": "E-Mail",
      "distribution_pattern": "US distribution to Louisiana",
      "recall_number": "Z-0620-2024",
      "product_description": "regard Operative LAP, Item Number 800943001; surgical convenience kit",
      "product_quantity": "345 units",
      "reason_for_recall": "Surgical convenience kits were manufactured with a component which was subsequently recalled by Nurse Assist.",
      "recall_initiation_date": "20231218",
      "center_classification_date": "20240112",
      "termination_date": "20241003",
      "report_date": "20240124",
      "code_info": "UDI/DI 10194717111863, Lot Numbers:  94792, 95613, 96003, 96845"
    }
  ]
}