{
  "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": "89951",
      "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": "Recall impacted one domestic consignee in NC",
      "recall_number": "Z-1051-2022",
      "product_description": "Regard brand CABG Pack A and B - Spartanburg",
      "product_quantity": "85 kits",
      "reason_for_recall": "Kits were packed into shipping boxes incorrectly.",
      "recall_initiation_date": "20220321",
      "center_classification_date": "20220509",
      "termination_date": "20231228",
      "report_date": "20220518",
      "code_info": "Item Number: 800208017, Lot 91156    UDI:  (01)10194717112495(17)230101(10)91156"
    }
  ]
}