{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79975",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution",
      "recall_number": "Z-1909-2018",
      "product_description": "Baxter EXACTAMIX Inlet, Vented, High-Volume Inlet, REF H938174    Usage:  Exacta-Mix 2400 Compounding System Administration set is a disposable component of a compounding device used in the pharmacy to compound multiple source ingredients into one final solution.",
      "product_quantity": "59475 units",
      "reason_for_recall": "Specific lots of EXACTAMIX Inlets listed below due to incorrectly performed over-labeling.  The inlets were over-labeled with a blank label, or with a label containing an extended expiration date. If the product is used beyond the expiration date,",
      "recall_initiation_date": "20180425",
      "center_classification_date": "20180522",
      "termination_date": "20201216",
      "report_date": "20180530",
      "code_info": "UDI:  00085412475790  Lot Numbers:  802279, 802280, 802281"
    }
  ]
}