{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77413",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "1450 E Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution to TN",
      "recall_number": "Z-2624-2017",
      "product_description": "LEGION(R) FEM CONE IMPACTOR HEADS:  a) REF 71441976, ID 18MM  b) REF 71441977, ID 20MM  c) REF 71441978, ID 22MM",
      "product_quantity": "36 units",
      "reason_for_recall": "The incorrect Loctite adhesive was used to assemble the impactor heads.",
      "recall_initiation_date": "20170530",
      "center_classification_date": "20170623",
      "termination_date": "20211210",
      "report_date": "20170705",
      "code_info": "Lot numbers:  a) 16HGA0031  b) 16HGA0034  c) 16HGA0035"
    }
  ]
}