{
  "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": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83520",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 NW 66th Ct",
      "address_2": "",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to AR, CA, FL, IL, IN, NY, SC, TX.",
      "recall_number": "Z-2499-2019",
      "product_description": "Threaded Offset Cup Impactor - Product Usage: To assist the surgeon in the implantation of Novation hip system components according to a conventional technique for total hip replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.",
      "product_quantity": "22 devices",
      "reason_for_recall": "The threaded mechanism of the Threaded Offset Cup Impactor may be gritty and difficult to turn potentially due to entrapped blast media.",
      "recall_initiation_date": "20190724",
      "center_classification_date": "20190910",
      "termination_date": "20230531",
      "report_date": "20190918",
      "code_info": "Catalog Number 181-02-01, Lot Numbers 103071001, UDI Number 10885862520623.    Expansion on 09/09/2019 to include Lot Number 8182001",
      "more_code_info": ""
    }
  ]
}