{
  "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": "89182",
      "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 in the countries of Australia, Austria, Belgium, Czech Republic, France, Germany, Ireland, Kazakhstan, Netherlands, Spain, United Kingdom. No US distribution.",
      "recall_number": "Z-0495-2022",
      "product_description": "LigaSure Blunt Tip Laparoscopic Sealer/Divider, Nano-Coated, Product Number LF1837",
      "product_quantity": "504 devices",
      "reason_for_recall": "Customers reported that the device jaws were difficult to open or would not open following application on tissue.  Use of a device with this potential assembly issue could result in the potential for bleeding, unintended tissue injury or loss, and delay in treatment while an alternate device is obtained.",
      "recall_initiation_date": "20211206",
      "center_classification_date": "20220113",
      "termination_date": "20230511",
      "report_date": "20220119",
      "code_info": "UDI: 20884521705880 10884521705883;  Lot Number: 11320187X"
    }
  ]
}