{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93306",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and Panama",
      "recall_number": "Z-0533-2024",
      "product_description": "Medline Leg bag, REF DYND12574",
      "product_quantity": "28942 devices",
      "reason_for_recall": "Undeclared latex",
      "recall_initiation_date": "20231019",
      "center_classification_date": "20231212",
      "report_date": "20231220",
      "code_info": "UDI/DI 40080196990338 (case), 10080196990337 (insert), Lot Numbers:  48623040001, 48623050001, 48623060001, 48623080001"
    }
  ]
}