{
  "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": [
    {
      "country": "United States",
      "city": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "the white printed paper layer on the pouch packaging  may not be fully adhered to the pouch foil layer. The upper paper layer may serve as a protective barrier and help support overall packaging.",
      "address_2": "",
      "product_quantity": "20,940 units",
      "code_info": "Lot Numbers:  GD894535, GD894550",
      "center_classification_date": "20140630",
      "distribution_pattern": "Distributed in the states of AR, TN MO, KS, TX, MS, and AL.",
      "state": "IL",
      "product_description": "Baxter, MiniCap with Povidone-Iodine solution, 5C4466P.  For dialysis.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-1945-2014",
      "initial_firm_notification": "",
      "product_type": "Devices",
      "event_id": "68640",
      "termination_date": "20140630",
      "more_code_info": "",
      "recall_initiation_date": "20130708",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}