{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89454",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of TN, TX.",
      "recall_number": "Z-0631-2022",
      "product_description": "ATTUNE REVISION POSTERIOR FEMORAL AUGMENT  SZ 9 12MM-intended as a Component  in total knee arthroplasty (TKA) revision surgeries  Product Number: 154909003",
      "product_quantity": "6 units",
      "reason_for_recall": "May have adhesive residue on the posterior surface of the femoral augment, if undetected prior to implantation, soft tissue irritation and/or infection may occur.",
      "recall_initiation_date": "20220105",
      "center_classification_date": "20220209",
      "termination_date": "20231222",
      "report_date": "20220216",
      "code_info": "Lots: JH9651, JH9649  GTIN: 10603295383178"
    }
  ]
}