{
  "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-1900-2016",
      "product_description": "Novation Ceramic AHS Cluster-Hole Shell, Plasma Coated, 54mm, O.D. (Acetabular Cup),  Catalog Number 140-01-54; For use in primary total hip arthroplasty.",
      "product_quantity": "3 devices",
      "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 Code: MRA;  Catalog Number 140-01-54, Serial Numbers: 4296076, 4296078, 4296079, Exp. 2/23/2021"
    }
  ]
}