{
  "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": "2026-09-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "event_date_initiated": "2002-11-01",
      "event_date_created": "2002-12-02",
      "city": "The",
      "address_1": "2828 North Cresent Ridge Dr",
      "reason_for_recall": "Separation between lid and housing unit.",
      "openfda": {},
      "recalling_firm": "Jostra-Bentley Corporation",
      "product_res_number": "Z-0312-03",
      "code_info": "Part Number C6918A4E (lots 63355 and 64015) Part Number C6918A3E (lots 63408, 63987, and 63988) Part Number C9315A2B (lot 63998) Part Number 60163301 (lot 64408, serial numbers starting with  7xxxxx)",
      "product_quantity": "356 units",
      "recall_status": "Completed",
      "res_event_number": "25002",
      "action": "Accounts notified by phone 10/9/02 and letter 11/1/02.  Recalling firm is requesting return of the recalled product.",
      "distribution_pattern": "OH, KY, AL, TN, FL, NY, IL, no government or military accounts",
      "state": "Woodlands",
      "product_description": "Spiral Gold Hollow Fiber Oxygenator with Duraflow Treatment, a hollow fiber membrane oxygenator.",
      "postal_code": "77381-3902"
    }
  ]
}