{
  "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": "Omaha",
      "state": "NE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88616",
      "recalling_firm": "Centese Inc.",
      "address_1": "4156 S 52nd St",
      "address_2": "N/A",
      "postal_code": "68117-1324",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution to a single consignee located in California.",
      "recall_number": "Z-0105-2022",
      "product_description": "Thoraguard Chest Tube Kit, 20 Fr",
      "product_quantity": "310 kits",
      "reason_for_recall": "An adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.",
      "recall_initiation_date": "20210831",
      "center_classification_date": "20211013",
      "termination_date": "20230807",
      "report_date": "20211020",
      "code_info": "Model: FGS-1126 Catalog Number: TGCT120020 Lot Numbers 20100102, 21031703, and 21053102"
    }
  ]
}