{
  "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": "2026-04-08",
    "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": "79600",
      "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": "E-Mail",
      "distribution_pattern": "USA (nationwide) Distribution to the states of : AL, AZ, CA, FL, GA, KS, MA, MD, MI, NC, NJ, NY, OH, PA, SC, TN, TX, VA, and WA",
      "recall_number": "Z-1462-2018",
      "product_description": "Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601    The knee system devices are sterile, single-use devices intended for us in revision total knee arthroplasty to alleviate pain and restore function.",
      "product_quantity": "77 total products",
      "reason_for_recall": "Customers may receive  the incorrect size implant from what is labeled on the box.",
      "recall_initiation_date": "20180130",
      "center_classification_date": "20180420",
      "termination_date": "20200507",
      "report_date": "20180502",
      "code_info": "Catalog #5545-A-301, lot code ER9WA1A, ER9WA1D, ER9WA1E  Catalog #5546-A-601, lot code ER9MA5A"
    }
  ]
}