{
  "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": "2026-10-21",
    "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": "99983",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the state of NY.",
      "recall_number": "Z-0189-2027",
      "product_description": "Medline convenience kit labeled as:  FOOT ANKLE. Medline Kit SKU DYNJ65395A",
      "product_quantity": "30 kits",
      "reason_for_recall": "Discrepancy in the shelf-life of a component",
      "recall_initiation_date": "20260911",
      "center_classification_date": "20261015",
      "report_date": "20261021",
      "code_info": "UDI/DI 10195327174156 (each) 40195327174157 (case), Lot Number 22GBW912",
      "more_code_info": ""
    }
  ]
}