{
  "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": "2026-04-01",
    "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": "88773",
      "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": "Worldwide distribution - US Nationwide distribution in the states of OK, TN and the country of Canada.",
      "recall_number": "Z-0143-2022",
      "product_description": "6.5MMX165MM CANNULATED SCREW",
      "product_quantity": "5 units",
      "reason_for_recall": "The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.",
      "recall_initiation_date": "20210920",
      "center_classification_date": "20211019",
      "termination_date": "20230324",
      "report_date": "20211027",
      "code_info": "Model 71106365S; Lot 20GT39417"
    }
  ]
}