{
  "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": "Verona",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89337",
      "recalling_firm": "Gentueri Inc",
      "address_1": "312 Locust Dr",
      "address_2": "N/A",
      "postal_code": "53593-2215",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of Indiana.",
      "recall_number": "Z-0504-2022",
      "product_description": "Gentueri Viral Transport Medium (VTM), Sterile, IVD",
      "product_quantity": "4,150 units",
      "reason_for_recall": "Medium showed visual turbidity and discoloration, potentially contaminating samples transported for testing.",
      "recall_initiation_date": "20210318",
      "center_classification_date": "20220118",
      "termination_date": "20230828",
      "report_date": "20220126",
      "code_info": "CAT #: 3300-000; Lot #: 1142"
    }
  ]
}