{
  "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": "80972",
      "recalling_firm": "MEDLINE INDUSTRIES INC",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States, Taiwan, Chile",
      "recall_number": "Z-0088-2019",
      "product_description": "Unna-Z: Unna Boot Compression Wrap with Zinc Oxide and Calamine, Item Numbers:  a) NONUNNA3 and b) NONUNNA4    Product is packaged in a foil pouch, which is inserted in a box carton.  There are 12 cartons in each case.",
      "product_quantity": "113,302 units",
      "reason_for_recall": "Firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.",
      "recall_initiation_date": "20180830",
      "center_classification_date": "20181006",
      "termination_date": "20230209",
      "report_date": "20181017",
      "code_info": "Lot numbers:  a) NONUNNA3: 70112, 70485, 70602, 80637, 80663, and 80719.  b) NONUNNA4: 70182, 70593, 80638, 80644, 80660, 80709 and 80712.",
      "more_code_info": ""
    }
  ]
}