{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Arlington",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74752",
      "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": "Belgium, Italy, Spain, and Poland",
      "recall_number": "Z-2588-2016",
      "product_description": "PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.",
      "product_quantity": "14 units",
      "reason_for_recall": "Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck).",
      "recall_initiation_date": "20160630",
      "center_classification_date": "20160818",
      "termination_date": "20170121",
      "report_date": "20160824",
      "code_info": "Lot number 1645222"
    }
  ]
}