{
  "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-1240-2017",
      "product_description": "Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702",
      "product_quantity": "2496",
      "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:  50525150  50386077  50261802  50197616  50178740  50171398  50158656  50138050  50121538  50103379  50089298  50082582  50061131"
    }
  ]
}