{
  "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": "Arlington",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70477",
      "recalling_firm": "Microport Orthopedics INC.",
      "address_1": "5677 Airline Rd",
      "address_2": "N/A",
      "postal_code": "38002-9501",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including AL, AZ, ID, KS, KS, MO, TX, IA, WV and Internationally to Canada and The Netherlands.",
      "recall_number": "Z-1249-2015",
      "product_description": "EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY, MicroPort Orthopedics, Inc.  Knee prosthesis component.",
      "product_quantity": "17 units",
      "reason_for_recall": "Some units of the EVOLUTION Tibial Base was affected by a casting tool issue which caused varying retaining wall thickness and keel offset in the finished product.",
      "recall_initiation_date": "20150202",
      "center_classification_date": "20150306",
      "termination_date": "20150319",
      "report_date": "20150318",
      "code_info": "Lot Numbers: 1560140, 15601401568897, 15601401570896"
    }
  ]
}