{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northbrook",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89051",
      "recalling_firm": "Luminex Corporation",
      "address_1": "4088 Commercial Ave",
      "address_2": "N/A",
      "postal_code": "60062-1829",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US:  TX, CT, LA",
      "recall_number": "Z-0920-2022",
      "product_description": "Verigene Processor SP, Model Numbers:  10-0000-07 and 10-0000-07-R",
      "product_quantity": "4 units",
      "reason_for_recall": "Two of three complaints were initiated due to the customers repeatedly obtaining No Call results on the Processor SPs in question.",
      "recall_initiation_date": "20190422",
      "center_classification_date": "20220413",
      "report_date": "20220420",
      "code_info": "Model Number 10-0000-07, Serial Numbers:  13042054,16347082,17215010;    Model Number 10-0000-07-R, Serial Numbers: 18079010"
    }
  ]
}