{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "142511",
      "product_res_number": "Z-0693-2016",
      "event_date_initiated": "2015-12-15",
      "event_date_posted": "2016-01-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2019-10-07",
      "res_event_number": "72926",
      "product_code": "FKX",
      "k_numbers": [
        "K043363",
        "K123630"
      ],
      "product_description": "Fresenius Liberty Cycler-Peritoneal Dialysis Cycler\nModel: 180111 and RTLR180111",
      "code_info": "All lot numbers",
      "firm_fei_number": "3001451489",
      "recalling_firm": "Fresenius Medical Care Renal Therapies Group, LLC",
      "address_1": "920 Winter St",
      "city": "Waltham",
      "state": "MA",
      "postal_code": "02451-1521",
      "additional_info_contact": "SAME\n781-699-9000",
      "reason_for_recall": "The door latch may not fully close and the door may open unexpectedly.  The door may make physical contact with anything near the door of the machine, including the patient.  May cause injury, delay in treatment, or Increased Intraperitoneal Volume (IIPV) (overfill).",
      "root_cause_description": "Device Design",
      "action": "Fresenius Medical Care issued on December 15, 2015, a n Important Product Notification to all affected customers informing them of the problem and how to recognize the proper latch closing. Questions regarding the contents of the Customer Notification or questions regarding the issue,  contact Technical Services at 1-800-227-2572 and reference the Field Action Number FA-2015-10-W.\nA reply form is included as part of the customer communication with\ninstructions to fill out and return via fax or scanned/emailed copy.",
      "product_quantity": "14,094 units",
      "distribution_pattern": "Nationwide Distribution",
      "openfda": {
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        ],
        "device_name": "System, Peritoneal, Automatic Delivery",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5630",
        "device_class": "2"
      }
    }
  ]
}