{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63126",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "345 E Main St",
      "address_2": "N/A",
      "postal_code": "46580-2746",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "USA (nationwide) including the states of Ohio, Carolinas and New England.",
      "recall_number": "Z-0386-2013",
      "product_description": "Trilogy II  Constrained Liner     The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.",
      "product_quantity": "1",
      "reason_for_recall": "Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons.  The product is packaged in the incorrect carton. Product labels and patient labels are correct, matching the product inside the carton.",
      "recall_initiation_date": "20120827",
      "center_classification_date": "20121120",
      "termination_date": "20130827",
      "report_date": "20121128",
      "code_info": "Item 00-6334-062-36, Lot 62023769"
    }
  ]
}