{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79166",
      "recalling_firm": "Covidien LLC",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Internationally, including Japan. No USA Customers",
      "recall_number": "Z-0908-2018",
      "product_description": "Endo GIA\" Radial Reload with Tri-Staple\" Technology    The Endo GIA  radial reloads with Tri-Staple  Technology have application in open or minimally invasive general abdominal, gynecologic and thoracic surgery for resection and transection of tissue and creation of anastomosis, as well as application deep in the pelvis, e.g. low anterior resection. They may be used for transection and resection of liver substance, hepatic vasculature and biliary structures and for transection and resection of pancreas.",
      "product_quantity": "163",
      "reason_for_recall": "The device cartridge disengaged during use due to manufacturing error.",
      "recall_initiation_date": "20170915",
      "center_classification_date": "20180305",
      "termination_date": "20181219",
      "report_date": "20180314",
      "code_info": "Product number: EGIARADXT  Lot code: N6L0351X"
    }
  ]
}