{
  "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": "2026-04-22",
    "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": "66355",
      "recalling_firm": "Medtronic Xomed, Inc.",
      "address_1": "6743 Southpoint Dr N",
      "address_2": "N/A",
      "postal_code": "32216-6218",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide Distribution (US), including the states of CA, NE, GA, and IL.",
      "recall_number": "Z-2284-2013",
      "product_description": "Universal Titanium Prosthesis, Round Head, with Flex H/A titanium shoe. The ear prosthesis is implantable and indicated for hearing loss.",
      "product_quantity": "60",
      "reason_for_recall": "One lot of the product was assembled using the Cam Head version of the same prosthesis instead of the Round head Shaft.",
      "recall_initiation_date": "20130823",
      "center_classification_date": "20130926",
      "termination_date": "20131107",
      "report_date": "20131002",
      "code_info": "REF: 1150000 Lot: 0207029284"
    }
  ]
}