{
  "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": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82426",
      "recalling_firm": "COVIDIEN LLC",
      "address_1": "15 Hampshire St",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (Nationwide) and to countries of: Canada, Chile, Costa Rica, Guatemala, Japan, Mexico, Panama, Slovakia, Spain, Switzerland and Turkey.",
      "recall_number": "Z-1212-2019",
      "product_description": "Covidien Endo Grasp Auto Suture Grasper 5mm  REF: 173030    The Covidien Endo Grasp\" Auto Suture\" grasper 5 mm instrument has applications in a variety of gynecologic, general, urologic, thoracic and endoscopic procedures for temporary grasping/clamping of tissue and small tubular structures.",
      "product_quantity": "240 units",
      "reason_for_recall": "Sterilization method used was not consistent with the labeling and the approved sterilization method",
      "recall_initiation_date": "20190313",
      "center_classification_date": "20190423",
      "termination_date": "20200423",
      "report_date": "20190501",
      "code_info": "Lot Numbers:  P8D1335PRX  P8D1336PRX  P8D1605PRX"
    }
  ]
}