{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lakewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68788",
      "recalling_firm": "Gambro Renal Products, Incorporated",
      "address_1": "14143 Denver West Pkwy",
      "address_2": "N/A",
      "postal_code": "80401-3266",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution.",
      "recall_number": "Z-2193-2014",
      "product_description": "Prismaflex TPE 2000 set, Product Number 1071441. Each set is packaged in a plastic pouch, 4 pouches per carton box",
      "product_quantity": "401,451",
      "reason_for_recall": "Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.",
      "recall_initiation_date": "20140718",
      "center_classification_date": "20140813",
      "termination_date": "20150205",
      "report_date": "20140820",
      "code_info": "Product Number 1071441. Batch number 12A1905 to 14C1706. Expiry date 01/2015 to 03/2017."
    }
  ]
}