{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Opelika",
      "state": "AL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69786",
      "recalling_firm": "Gambro Renal Products Inc",
      "address_1": "1101 Jeter Ave",
      "address_2": "N/A",
      "postal_code": "36801-3885",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including PR, and countries of: CA, BB, BM, BS, DO and LC.",
      "recall_number": "Z-0490-2015",
      "product_description": "Polyflux Revaclear Max Dialyzer, Model Number 110634.    The Polyflux Revaclear¿ and Polyflux Revaclear¿ Max Dialyzers are single use devices intended for the treatment of acute and chronic renal failure by hemodialysis.",
      "product_quantity": "20 million dialyzers",
      "reason_for_recall": "Gambro is initiating a field action for Polyflux Revaclear Dialyzer and Polyflux Revaclear Max Dialyzer due to potential tears in the individual packaging that may compromise the sterile barrier.",
      "recall_initiation_date": "20141105",
      "center_classification_date": "20141201",
      "termination_date": "20150520",
      "report_date": "20141210",
      "code_info": "Lot No C412207001 to C412209101, C413200101 to C413206001, C414200101 to C414206001"
    }
  ]
}