{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "A leak may allow for microbial contamination of the sterile fluid path.",
      "address_2": "",
      "product_quantity": "29,088 units",
      "code_info": "Product Code 2J8003, Lot No. DR16J18096.",
      "center_classification_date": "20180129",
      "distribution_pattern": "Distribution in the US and Canada.",
      "state": "IL",
      "product_description": "Empty IntraVia Container with Non-DEHP Fluid Path, 500mL    Containers are intended for use in the preparation and administration of drug admixtures.",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corporation",
      "recall_number": "Z-0485-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78042",
      "termination_date": "20201103",
      "more_code_info": "",
      "recall_initiation_date": "20170727",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}