{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Blue Ash",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88349",
      "recalling_firm": "Ethicon Endo-Surgery Inc",
      "address_1": "4545 Creek Rd",
      "address_2": "N/A",
      "postal_code": "45242-2803",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of MD, WA and the countries of Belgium, China, Denmark, Estonia, France, Germany, Italy, Japan, Korea,  Latvia, Lithuania, Netherlands, Poland, Portugal, Russia, Spain, Sweden, Switzerland,  United Kingdom.",
      "recall_number": "Z-2326-2021",
      "product_description": "ECHELON FLEX Powered Plus Stapler-intended for transection, resection, and/or creation of anastomoses. The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic, and pediatric surgical procedures.  Product Code: PSEE60A",
      "product_quantity": "763 eaches",
      "reason_for_recall": "Mislabeled: Labeled on the package as 60mm contains  45mm devices",
      "recall_initiation_date": "20210603",
      "center_classification_date": "20210819",
      "termination_date": "20220914",
      "report_date": "20210825",
      "code_info": "Lot U94V47  Exp Date: July 31, 2023  GTIN: 10705036014607"
    }
  ]
}