{
  "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": "84530",
      "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": "Letter",
      "distribution_pattern": "Nationwide  Foreign: GHANA",
      "recall_number": "Z-1072-2020",
      "product_description": "Centurion-Vaginal Speculum  VS2000LST\tSTERILE ER VAGINAL SPECULUM  W/LIGHT",
      "product_quantity": "1100",
      "reason_for_recall": "Incomplete seals on the sterile package may compromise the sterility",
      "recall_initiation_date": "20191211",
      "center_classification_date": "20200205",
      "termination_date": "20200904",
      "report_date": "20200212",
      "code_info": "VS2000LST STERILE ER VAGINAL SPECULUM  W/LIGHT  2019021290"
    }
  ]
}