{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93503",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0657-2024",
      "product_description": "Baxter Coseal Premix, Surgical Sealant, Product Codes:  a)  934070;  b)  934071;   c)  934072",
      "product_quantity": "",
      "reason_for_recall": "Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products\u0019 Instructions for Use (IFU) or Prescribing Information (PI).",
      "recall_initiation_date": "20231206",
      "center_classification_date": "20240105",
      "report_date": "20240117",
      "code_info": "All serial numbers a) Product code 934070, UDI/DI 5413765404610;  b) Product code 934071, UDI/DI 5413765404627;  c) Product code 934072, have no UDI/DI.",
      "more_code_info": ""
    }
  ]
}