{
  "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": "2026-04-01",
    "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": "89151",
      "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 Nationwide distribution in the state of California.",
      "recall_number": "Z-0554-2022",
      "product_description": "HARDY DIAGNOSTICS CatScreen, 25dsk/vial",
      "product_quantity": "100 units (4 packs, 25 per pack)",
      "reason_for_recall": "Product stored incorrectly in temperature controlled setting instead of refrigeration.",
      "recall_initiation_date": "20211201",
      "center_classification_date": "20220202",
      "termination_date": "20230109",
      "report_date": "20220209",
      "code_info": "Model Number HADZ110, all lots"
    }
  ]
}