{
  "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": "86626",
      "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 Nationwide distribution in the states of MO and OK.",
      "recall_number": "Z-0524-2021",
      "product_description": "Regard - Product Usage: Obstetric Gynecologic specialized manual instrument. Labor and delivery kits.",
      "product_quantity": "220 kits",
      "reason_for_recall": "Labeling error, incorrect expiration date.",
      "recall_initiation_date": "20201012",
      "center_classification_date": "20201202",
      "termination_date": "20210513",
      "report_date": "20201209",
      "code_info": "Lot Numbers: 78483C, 79932C, 81043C, 82586C, 83090C.",
      "more_code_info": ""
    }
  ]
}