{
  "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-1244-2017",
      "product_description": "Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706",
      "product_quantity": "1410",
      "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:  50439354  50393992  50252777  50208023  50171402  50138054  50103142  50066114  576304"
    }
  ]
}