{
  "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": "Verona",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89336",
      "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": "Domestic: Illinois, Nebraska, and Wisconsin.",
      "recall_number": "Z-0561-2022",
      "product_description": "Gentueri Viral Transport Medium Kit with 8cm Breakpoint Swab",
      "product_quantity": "13,975 units (2 mL in a 15 mL conical tube)",
      "reason_for_recall": "Kits failed sterility testing and showed evidence of contamination.",
      "recall_initiation_date": "20200706",
      "center_classification_date": "20220204",
      "termination_date": "20231212",
      "report_date": "20220216",
      "code_info": "CAT#: 3300-000; Lot No.: 1029."
    }
  ]
}