{
  "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": "69644",
      "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": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.",
      "recall_number": "Z-0515-2015",
      "product_description": "Total Temporomandibular Joint Replacement System- 50mm Rt Narrow Ti Mand  Reconstruction of the temporomandibular joint",
      "product_quantity": "42",
      "reason_for_recall": "Laser etching on the parts is wider and deeper than the conditions previously validated.",
      "recall_initiation_date": "20141017",
      "center_classification_date": "20141208",
      "termination_date": "20170104",
      "report_date": "20141217",
      "code_info": "Model 01-6550TI, Lot #s: 531890A, 531890B, 531900A, 531900B, 544220B, 544230A, 544230B, 544200A, 544200B, 544210A, 544210B, 544220A."
    }
  ]
}