{
  "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": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78360",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "Three Lakes Drive",
      "address_2": "N/A",
      "postal_code": "60093",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of AK, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, NC, NH, NJ, NY, OH, OK, OR, PA, TN, TX, WA and the countries of Canada, Saudi Arabia, and Netherlands.",
      "recall_number": "Z-0295-2018",
      "product_description": "Sterile Elastic Esmark Bandage, 3\" x 9\", individually packaged in a Tyvek plastic form fill seal pouch and placed into a corrugate case, 20 individually packed bandages per case.",
      "product_quantity": "5,722 units total",
      "reason_for_recall": "Product did not undergo correct sterilization procedures and may potentially be non-sterile.",
      "recall_initiation_date": "20170718",
      "center_classification_date": "20171228",
      "termination_date": "20200424",
      "report_date": "20180103",
      "code_info": "Model No. DYNJ05914, Lots: 17GB3101, 172B2025, 17FB9612, 17QB8614"
    }
  ]
}