{
  "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-2625-2017",
      "product_description": "LEGION(R) TIB CONE IMPACTOR HEADS:  a) REF 71441972, ID 24MM  b) REF 71441971, ID 22MM  c) REF 71441973, ID 26MM  d) REF 71441974, ID 28MM  e) REF 71441975, ID 30MM",
      "product_quantity": "46 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) 16HGA0040  b) 16JGA0003  c) 16JGA0005  d) 16JGA0006  e) 16JGA0007"
    }
  ]
}