{
  "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": "Jacksonville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72366",
      "recalling_firm": "Biomet Microfixation, LLC",
      "address_1": "1520 Tradeport Dr",
      "address_2": "N/A",
      "postal_code": "32218-2480",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution including CA, FL, OK, NY, NC, and IL.",
      "recall_number": "Z-0136-2016",
      "product_description": "Neuro Combo Set Case  The cases hold surgical instrumentation in place during handling and storage.",
      "product_quantity": "37 cases",
      "reason_for_recall": "The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force.",
      "recall_initiation_date": "20150806",
      "center_classification_date": "20151020",
      "termination_date": "20171013",
      "report_date": "20151028",
      "code_info": "Lot Code # 101337 Model # 17-5000"
    }
  ]
}