{
  "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": "2026-07-01",
    "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": "88413",
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "address_1": "700 Orthopaedic Dr",
      "address_2": "N/A",
      "postal_code": "46582-3994",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in the countries of Canada, France.",
      "recall_number": "Z-2348-2021",
      "product_description": "ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty   Part Number: 1512-16-080",
      "product_quantity": "7 units",
      "reason_for_recall": "Package labeled as 16mm x 80mm contained a 16mm x 130mm stem instead and result in obtaining a replacement",
      "recall_initiation_date": "20210701",
      "center_classification_date": "20210825",
      "termination_date": "20230201",
      "report_date": "20210901",
      "code_info": "Lot Number: J82N61 Expiry Date: 31May2030 GTIN: 10603295043010"
    }
  ]
}