{
  "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": [
    {
      "country": "United States",
      "city": "Blue Ash",
      "address_1": "4545 Creek Rd",
      "reason_for_recall": "The staplers may contain an out of specification anvil component within the jaw of the device.  This condition may lead to malformed staples, which can compromise staple line integrity.  If the staple line is compromised, there is a potential risk of prolonged surgery, postoperative anastomotic leak, hemorrhage, hemorrhagic shock, additional surgical intervention, or death.",
      "address_2": "",
      "product_quantity": "849 units",
      "code_info": "Lot: T9408M,   T94899,   T94A9Z",
      "center_classification_date": "20191029",
      "distribution_pattern": "Worldwide distribution.  US Nationwide.  Belgium, Brazil, Canada, Chile, Colombia, Japan, Kuwait, Saudi Arabia, and Singapore.",
      "state": "OH",
      "product_description": "ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft, Product Code EC60A",
      "report_date": "20191106",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Ethicon Endo-Surgery Inc",
      "recall_number": "Z-0200-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83897",
      "termination_date": "20210603",
      "more_code_info": "",
      "recall_initiation_date": "20191003",
      "postal_code": "45242-2803",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}