{
  "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": [
    {
      "country": "United States",
      "city": "Memphis",
      "address_1": "1450 E. Brooks Rd",
      "reason_for_recall": "Inner spherical radius of the shell is undersized.",
      "address_2": "",
      "product_quantity": "10 units",
      "code_info": "Batch No. 13EM03053",
      "center_classification_date": "20140221",
      "distribution_pattern": "Worldwide Distribution: US Distribution to NJ and FL; and the countries of: Colombia and Costa Rica.",
      "state": "TN",
      "product_description": "Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc.    Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.",
      "report_date": "20140305",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smith & Nephew Inc",
      "recall_number": "Z-1066-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "67404",
      "termination_date": "20161115",
      "more_code_info": "",
      "recall_initiation_date": "20140123",
      "postal_code": "38116",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}