{
  "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": "76414",
      "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": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru,   Singapore, Venezuela",
      "recall_number": "Z-1239-2017",
      "product_description": "Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701",
      "product_quantity": "2646",
      "reason_for_recall": "The single use devices are provided sterile and do not have an expiration date on the label.",
      "recall_initiation_date": "20170202",
      "center_classification_date": "20170222",
      "termination_date": "20190920",
      "report_date": "20170301",
      "code_info": "Batch Numbers:  50586138  50458123  50418120  50339534  50306882  50285907  50248565  50231427  50197615  50171397  50158655  50138049  50119457  50089297  50082581  50069485"
    }
  ]
}