{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93507",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 Nw 66th Ct",
      "address_2": "N/A",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US NY, TX, IN, IL, MN, KY, VA, MD, TN, GA, NH, ME, SC, NV, FL, AR and Australia, Brazil, Chile, France, Germany, Guatemala, Italy, Japan, Korea, Slovenia, Spain, UK",
      "recall_number": "Z-0583-2024",
      "product_description": "Exactech Optetrak Logic Knee System, Catalog Numbers:    a) 02-012-47-3011,   b) 02-012-47-5009,   c) 02-012-47-5011,   d) 02-012-65-3013",
      "product_quantity": "N/A",
      "reason_for_recall": "Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.",
      "recall_initiation_date": "20231121",
      "center_classification_date": "20231219",
      "report_date": "20231227",
      "code_info": "a) 02-012-47-3011, GTIN 10885862174352, Serial Numbers:  A676497;  b) 02-012-47-5009, GTIN 10885862174543, Serial Numbers:  A641353;   c) 02-012-47-5011, GTIN 10885862174550, Serial Numbers:  A641341;  d) 02-012-65-3013, GTIN 10885862613400, Serial Numbers:  A655561"
    }
  ]
}