{
  "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": "Round Lake",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63898",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "Route 120 And Wilson Rd",
      "address_2": "N/A",
      "postal_code": "60073-9799",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including FL, GA, IL, KS, KY, MI, MO, NC, ND, OH, PA, SC, TN, TX, WV, Puerto Rico and Internationally  to Canada.",
      "recall_number": "Z-2687-2016",
      "product_description": "Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single use nonpyrogenic fluid pathway; 50 sets per case;   For the administration of drugs and solutions to a patient's vascular system through a vascular access device.",
      "product_quantity": "15,257 units",
      "reason_for_recall": "Some of the individual extension set packages were improperly sealed, compromising the sterility of the product.",
      "recall_initiation_date": "20121214",
      "center_classification_date": "20160829",
      "termination_date": "20161223",
      "report_date": "20160907",
      "code_info": "product code 2N3345, lot number UR12E03108"
    }
  ]
}