{
  "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": "Mundelein",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76132",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "1 Medline Pl",
      "address_2": "N/A",
      "postal_code": "60060-4485",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and to the countries of : Chile, Peru, El Salvador and Taiwan.",
      "recall_number": "Z-1074-2017",
      "product_description": "Unna-Z, Unna Boot with Zinc and Calamine, Compression Wrap, 1 Per Box, 3-4in x 10yds",
      "product_quantity": "117,059 units",
      "reason_for_recall": "Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3\u001dX10\u001d and Unna Z Unna Boot Bandage 4\u001dX10\u001d due to contamination of the products with common mold (Cladosporium sphaerospermum/cladosporioides/herbarum/phaenocomae/halotolerans and Penicillium corylophilum)..",
      "recall_initiation_date": "20161123",
      "center_classification_date": "20170123",
      "termination_date": "20190719",
      "report_date": "20170201",
      "code_info": "Unit Numbers: NONUNNA3 & NONUNNA4  Lot Numbers: 52581 through 63599"
    }
  ]
}