{
  "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": "Cirencester",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91039",
      "recalling_firm": "Corin Ltd",
      "address_1": "Unit 1-57-8",
      "address_2": "Corinium Centre",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Distribution in the US to New Jersy and Puerto Rico.  International distribution to South Africa and France.",
      "recall_number": "Z-0273-2023",
      "product_description": "Unity Total Knee System.      Used for knee prosthesis in total knee replacement",
      "product_quantity": "4 devices",
      "reason_for_recall": "The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging.",
      "recall_initiation_date": "20221031",
      "center_classification_date": "20221121",
      "termination_date": "20240112",
      "report_date": "20221130",
      "code_info": "Model Number: 112.040.06; Lot Number: 504337"
    }
  ]
}