{
  "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": "Inchinnan",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88278",
      "recalling_firm": "Vascutek, Ltd.",
      "address_1": "Newmains Avenue",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution was made to PR and Guam.",
      "recall_number": "Z-2543-2021",
      "product_description": "The Instructions for Use (IFU) for:  Carotid Patch and Gelsoft Patch vascular patches.      FSN says Tapered Carotid Patch 920875t",
      "product_quantity": "159 total vascular grafts and patches",
      "reason_for_recall": "The devices contained the IFU for distribution to ROW (rest of world) consignees rather than U.S. consignees.",
      "recall_initiation_date": "20210708",
      "center_classification_date": "20210924",
      "termination_date": "20240819",
      "report_date": "20211006",
      "code_info": "To be reported."
    }
  ]
}