{
  "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": "Solon",
      "address_1": "31200 Solon Rd",
      "reason_for_recall": "To correct software bugs that could affect the ability to accurately measure fluid deficit.",
      "address_2": "Unit 1",
      "product_quantity": "127 units",
      "code_info": "Serial Numbers 20100001 through 20140044",
      "center_classification_date": "20150420",
      "distribution_pattern": "US Distribution to the states of : OH, MS, MA, WA, MI, NC, NY, WV, LA, TX  and IL.",
      "state": "OH",
      "product_description": "Fluid Management System P4000;  for irrigation and fluid warming in laparoscopic procedures, and distention, fluid warming, and volume/deficit measurements in endoscopic procedures within gynecology, urology, and orthopedic procedures.",
      "report_date": "20150429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Thermedx LLC",
      "recall_number": "Z-1463-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69996",
      "termination_date": "20150914",
      "more_code_info": "",
      "recall_initiation_date": "20140901",
      "postal_code": "44139-3556",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}