{
  "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": "89471",
      "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": "E-Mail",
      "distribution_pattern": "Missouri",
      "recall_number": "Z-0693-2022",
      "product_description": "Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile",
      "product_quantity": "50 kits",
      "reason_for_recall": "Products are mislabeled with the incorrect product identification on individual kit labeling.",
      "recall_initiation_date": "20220113",
      "center_classification_date": "20220228",
      "termination_date": "20220928",
      "report_date": "20220309",
      "code_info": "Item No. 8800297010; Lot No. 90328; UDI 10194717113164",
      "more_code_info": ""
    }
  ]
}