{
  "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": "2026-04-15",
    "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": "73200",
      "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": "Letter",
      "distribution_pattern": "Distributed in FL, NJ, NY, OH, OK, RI, TN, VA and HI.",
      "recall_number": "Z-1904-2016",
      "product_description": "Novation Press-Fit Tapered, Standard Offset, HA Coated, 12/14 Taper,  Femoral Stem;  Catalog Number 160-10-16; For use in primary total hip arthroplasty.",
      "product_quantity": "1 device.",
      "reason_for_recall": "Devices were inadvertently sent to packaging and finished goods prior to the PMA site-change supplement approval.",
      "recall_initiation_date": "20160412",
      "center_classification_date": "20160602",
      "termination_date": "20190724",
      "report_date": "20160608",
      "code_info": "Product Codes:  LPH, MEH, LWJ, JDI;  Catalog Number 160-10-16, Serial Number: 4256338, Exp. 1/27/2021."
    }
  ]
}