{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tampa",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73205",
      "recalling_firm": "Corin USA Limited",
      "address_1": "5670 W Cypress St Ste C",
      "address_2": "N/A",
      "postal_code": "33607-1774",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of CA, FL, ID, TX, OK, OH, MA, and NC and the countries of Australia Belgium, Egypt, Germany, Ghana, Italy,  Japan, Poland, South Africa and UK.",
      "recall_number": "Z-1528-2016",
      "product_description": "Trinity Acetabular Shell    Product Usage Total Hip Replacement.",
      "product_quantity": "629 devices in total",
      "reason_for_recall": "Potential for abrasion of the sterile barrier pouches of the new packaging system.",
      "recall_initiation_date": "20160129",
      "center_classification_date": "20160422",
      "termination_date": "20191216",
      "report_date": "20160504",
      "code_info": "No Hole Shell 048mm Taper Size 2,  Lot Codes: 322986, 323743, 320026, 322977,  323744;  No Hole Shell 052mm Taper Size 3, Lot Codes: 322396, 322971, 322403, 322984, 322985, 323750."
    }
  ]
}