{
  "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-0588-2024",
      "product_description": "Exactech Vantage Mobile Bearing Tibial Inserts, Catalog Numbers:    a)\t350-41-23,   b)\t350-42-03",
      "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) 350-41-23, GTIN none, Serial Numbers:  A658148;  b) 350-42-03, GTIN none, Serial Numbers:  A688867, A688880, A688864, A688868, A688870, A688872, A688873, A688876, A688879, A688881, A688882"
    }
  ]
}