{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67042",
      "recalling_firm": "Smith & Nephew Inc",
      "address_1": "1450 E. Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed in China and Spain.",
      "recall_number": "Z-0581-2014",
      "product_description": "REFLECTION(R), MICROSTABLE(R), ACETABULAR LINER, 20o OVERHANG, 28 MM ID, 54-56 OD, QTY: (1), STERILE EO, REF 71742854, Smith & Nephew, Inc. Memphis, TN 38116 USA.    Orthopaedic.",
      "product_quantity": "38 units",
      "reason_for_recall": "One batch of the Reflection(TM) Polyethylene Acetabular Liners may be out of tolerance causing the liner not to fully seat into the shell.",
      "recall_initiation_date": "20131125",
      "center_classification_date": "20131226",
      "termination_date": "20170201",
      "report_date": "20140101",
      "code_info": "Batch No. 12BM04836",
      "more_code_info": ""
    }
  ]
}