{
  "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": "Ongoing",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82950",
      "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": "Nationwide domestic distribution, worldwide foreign distribution.",
      "recall_number": "Z-1825-2019",
      "product_description": "EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT",
      "product_quantity": "3,113,280",
      "reason_for_recall": "The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.",
      "recall_initiation_date": "20190517",
      "center_classification_date": "20190615",
      "report_date": "20190626",
      "code_info": "lots N5A0871KX  N7A0527KX  N7E0441KX  N8J0039KX  N8J0527KX  N8J0820KX"
    }
  ]
}