{
  "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": "Greer",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "75415",
      "recalling_firm": "North American Rescue LLC.",
      "address_1": "35 Tedwall Ct",
      "address_2": "N/A",
      "postal_code": "29650-4791",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, Australia & Switzerland",
      "recall_number": "D-0180-2017",
      "product_description": "Amphibious Trauma Kit - Product Code 85-0639,  North American Rescue",
      "product_quantity": "unknown",
      "reason_for_recall": "Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.",
      "recall_initiation_date": "20160927",
      "center_classification_date": "20161208",
      "termination_date": "20170309",
      "report_date": "20161214",
      "code_info": "Kit Part # 85-0639 - Kit Lot # 85-0639080516, 85-0639060116, 85-0639061016, 85-0639071416, 85-0639072116, 85-0639050316, 85-0639050416, 85-0639051316, 85-0639082216, 85-0639090116, 85-0639091316"
    }
  ]
}