{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Farnham",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "95820",
      "recalling_firm": "Biocompatibles UK, Ltd.",
      "address_1": "Chapman House",
      "address_2": "Farnham Business Park; Weydon Lane",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-0113-2025",
      "product_description": "Varithena (polidocanol injectable foam) Administration Pack, Contains: 3 silicone-free syringes, 2 compression pads, 1 Varithena Transfer Unit, 1 manometer tubing, Rx Only, Distributed by Biocompatibles Inc., a BTG International Group company. CN01114.3",
      "product_quantity": "432 administration packs",
      "reason_for_recall": "Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer Lock Solo syringes packaged in the pack, instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes (luer slip connection).",
      "recall_initiation_date": "20240815",
      "center_classification_date": "20241206",
      "termination_date": "20250221",
      "report_date": "20241218",
      "code_info": "Lot # 34067418, Exp. March 2026, 34067419, Exp. March 2026",
      "more_code_info": ""
    }
  ]
}