{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Arlington",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91102",
      "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": "E-Mail",
      "distribution_pattern": "International Distribution to countries of: Germany, Italy, France, Belgium, Austria, Greece, Romania, Japan, and P.R. China.",
      "recall_number": "Z-0276-2023",
      "product_description": "EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base",
      "product_quantity": "22 units",
      "reason_for_recall": "One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging.",
      "recall_initiation_date": "20221028",
      "center_classification_date": "20221122",
      "report_date": "20230222",
      "code_info": "UDI/DI 0 0192629 08293 9, Lot 1916715"
    }
  ]
}