{
  "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": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79661",
      "recalling_firm": "Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Affected products were sent to three medical facilities.  Affected product will be returned to the manufacturer for disposition.",
      "recall_number": "Z-1512-2018",
      "product_description": "Knee Prosthesis, Sterile, Single-Use devices    Product Usage:  The knee system devices are intended for use in revision total knee arthroplasty to alleviate pain and restore function",
      "product_quantity": "6 units of catalog 5521-B-400",
      "reason_for_recall": "Firm became aware that the specific product/lot combinations referenced above may contain the incorrect size implant from what is labeled on the box.",
      "recall_initiation_date": "20180112",
      "center_classification_date": "20180424",
      "termination_date": "20200507",
      "report_date": "20180502",
      "code_info": "Catalog 5521-B-300, lot code ATV7IA  Catalog 5521-B-400, lot code ATY40A"
    }
  ]
}