{
  "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": "Leeds",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90801",
      "recalling_firm": "Surgical Innovations Ltd",
      "address_1": "6 Clayton Wood Bank",
      "address_2": "Lds",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: MA",
      "recall_number": "Z-1852-2022",
      "product_description": "Product/Part:    YelloPort Elite 12x75 Pencil Point Trocar/ET1207503;    YelloPort Elite Hasson Adaptor 10mm/EA10NH.  For use in laparoscopic procedures.",
      "product_quantity": "19",
      "reason_for_recall": "Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.",
      "recall_initiation_date": "20220120",
      "center_classification_date": "20220929",
      "report_date": "20221005",
      "code_info": "Part/UDI-DI/Lot: ET1207503/05051986012438/735479, EA10NH/05051986012100/734029"
    }
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}