{
  "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": "Williamston",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84165",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "100 Centurion Way",
      "address_2": "N/A",
      "postal_code": "48895-9086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0344-2020",
      "product_description": "Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG  Code: DT11955",
      "product_quantity": "80 units",
      "reason_for_recall": "Sterile packaging incomplete seals may compromise sterility of the product",
      "recall_initiation_date": "20191024",
      "center_classification_date": "20191106",
      "termination_date": "20200624",
      "report_date": "20191113",
      "code_info": "Lot/Batch Number: 2019052190  Exp Date: 5/31/2024"
    }
  ]
}