{
  "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": "69586",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including GA, MA, NC, NY, PA, and WA.",
      "recall_number": "Z-0932-2015",
      "product_description": "Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis.",
      "product_quantity": "55 units",
      "reason_for_recall": "System error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger.",
      "recall_initiation_date": "20140424",
      "center_classification_date": "20150107",
      "termination_date": "20170721",
      "report_date": "20150114",
      "code_info": "Product Code: 5C9310",
      "more_code_info": ""
    }
  ]
}