{
  "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": [
    {
      "country": "United States",
      "city": "Jacksonville",
      "address_1": "1520 Tradeport Dr",
      "reason_for_recall": "Potential sterility deficiency.",
      "address_2": "",
      "product_quantity": "54 units",
      "code_info": "Custom made, one per customer. Affected units were sealed between April 28, 2016 and June 7, 2016",
      "center_classification_date": "20160908",
      "distribution_pattern": "Worldwide Distribution - US including AZ, CA, FL, MO, NH, PA, TX, & VA, and Internationally to Austria, Canada, England, Germany, Greece, Italy, Netherlands, & South Africa.",
      "state": "FL",
      "product_description": "Hard Tissue Replacement (HTR) Implant, Rx only, for use in single procedure only. Custom made.  HTR polymer implants are intended for bone replacement/augmentation for treatment of craniofacial voids/defects resulting from disease, injury, or surgical trauma.",
      "report_date": "20160914",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet Microfixation, LLC",
      "recall_number": "Z-2751-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74798",
      "termination_date": "20190821",
      "more_code_info": "",
      "recall_initiation_date": "20160613",
      "postal_code": "32218-2480",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}