{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Completed",
      "city": "Leeds",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90447",
      "recalling_firm": "Surgical Innovations  Ltd",
      "address_1": "Clayton House",
      "address_2": "6 Clayton Wood Rise",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of FL, IN, WA, MA and the countries of Armenia, Australia, Austria, Belgium, Canada, Croatia, Cyprus, Czech Republic, Ecuador, UK, Finland, France, Germany, Greece, Hong Kong, Hungary, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Malaysia, Mexico, N. Ireland, Norway, Poland, Russia, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and Dubai.",
      "recall_number": "Z-1396-2022",
      "product_description": "YelloPort Elite Universal Seal. For use in laparoscopic procedures.",
      "product_quantity": "N/A",
      "reason_for_recall": "There is the potential that YelloPort Elite Universal Seals packaging may contain small holes which may affect the sterility of the product.",
      "recall_initiation_date": "20220602",
      "center_classification_date": "20220718",
      "report_date": "20220727",
      "code_info": "All Lots; UDI/DI:05051986001562"
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}