{
  "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": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88369",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "1 Scimed Pl",
      "address_2": "N/A",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Belgium, Canada, Germany, Spain, France, United Kingdom/Great Britain, Hong Kong, Ireland, Israel, India, Italy, Netherlands, Poland, Portugal, Saudi Arabia, Singapore, Switzerland, Turkey, and Argentina.",
      "recall_number": "Z-2327-2021",
      "product_description": "TheraSphere Administration Set, REF OTT-SPE-FP-226 (990226.SPE)",
      "product_quantity": "4980 sets",
      "reason_for_recall": "Potential for leaks and loosening at the patient catheter connection",
      "recall_initiation_date": "20210723",
      "center_classification_date": "20210819",
      "report_date": "20210825",
      "code_info": "GTIN 05060116920253, Lot Numbers:  001E, 002E, 004E, 005E, 006E, 007E, 114E, 690E, 692E"
    }
  ]
}