{
  "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": [
    {
      "country": "United States",
      "city": "Buffalo Grove",
      "address_1": "1700 Leider Ln",
      "reason_for_recall": "Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shock.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "Serial Number  102",
      "center_classification_date": "20181003",
      "distribution_pattern": "Distribution in US state of MO.",
      "state": "IL",
      "product_description": "Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microscopic analysis for medical diagnostics.",
      "report_date": "20181010",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Leica Microsystems, Inc.",
      "recall_number": "Z-0019-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80986",
      "termination_date": "20200710",
      "more_code_info": "",
      "recall_initiation_date": "20180904",
      "postal_code": "60089-6622",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}