{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90870",
      "recalling_firm": "BALT USA, LLC",
      "address_1": "29 Parker Ste 100",
      "address_2": "N/A",
      "postal_code": "92618-1667",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - U.S. Nationwide distribution in the states of FL, GA, NC, and PA. The countries of Dominican Republic, India and Japan.",
      "recall_number": "Z-0103-2023",
      "product_description": "Optima Coil System      Model Number OPTI0208CSS10,     Model Number OPTI0308CSS10. Used in endovascular procedures.",
      "product_quantity": "41 impacted devices",
      "reason_for_recall": "Product pouch label does not match up with carton label",
      "recall_initiation_date": "20220907",
      "center_classification_date": "20221020",
      "report_date": "20221026",
      "code_info": "Model Number: OPTI0208CSS10 UDI-DI Code: 00818053025815 Lot Number: F220601068  Model Number: OPTI0308CSS10 UDI-DI Code: 00818053025891 Lot Number: F220601089",
      "more_code_info": ""
    }
  ]
}