{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hayward",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74139",
      "recalling_firm": "Baxter Healthcare Corp",
      "address_1": "21026 Alexander Ct",
      "address_2": "N/A",
      "postal_code": "94545-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed US (nationwide) including Puerto Rico and in the Bahamas, Canada, and Singapore.",
      "recall_number": "Z-1839-2016",
      "product_description": "COSEAL Surgical Sealant Kit, 4 mL, Product Code: 934071;  For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.",
      "product_quantity": "6,804 units",
      "reason_for_recall": "Potential for incomplete dissolution of the polyethylene glycol (PEG) component during the reconstitution of the product, which may affect the consistency of the hydrogel formation during use.",
      "recall_initiation_date": "20160512",
      "center_classification_date": "20160531",
      "termination_date": "20170323",
      "report_date": "20160608",
      "code_info": "HA160151, HA151205, HA151036, HA151035, HA160229"
    }
  ]
}