{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Tonbridge",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85214",
      "recalling_firm": "Boddingtons Plastics Ltd",
      "address_1": "Wheelbarrow Park Estate",
      "address_2": "Pattenden Lane",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide  Foreign:",
      "recall_number": "Z-1718-2020",
      "product_description": "Endocuff Vision: models ARV  110, 120, 130, 140   Intended Use: ENDOCUFF VISION is a device attached to the distal end of a colonoscope, designed to maintain and maximize the viewable mucosa during endocosopic therapy by manipulating colonic folds",
      "product_quantity": "13202  Units US",
      "reason_for_recall": "Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)",
      "recall_initiation_date": "20200311",
      "center_classification_date": "20200416",
      "termination_date": "20220810",
      "report_date": "20200422",
      "code_info": "All batches distributed prior to 1st May 2020.",
      "more_code_info": ""
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}