{
  "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": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78752",
      "recalling_firm": "Phadia US Inc",
      "address_1": "4169 Commercial Ave",
      "address_2": "N/A",
      "postal_code": "49002-9701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0387-2018",
      "product_description": "Phadia 1000 Instrument, Article Number 12-3800-01.",
      "product_quantity": "70 units",
      "reason_for_recall": "The \"Retry\" command does not function properly which could cause a shortage of Wash and Rinse solution and affect assay performance and test results.",
      "recall_initiation_date": "20170705",
      "center_classification_date": "20180118",
      "termination_date": "20181004",
      "report_date": "20180124",
      "code_info": "All versions of the instrument"
    }
  ]
}