{
  "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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    {
      "status": "Completed",
      "city": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86777",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "1 Scimed Pl",
      "address_2": "N/A",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0674-2021",
      "product_description": "IceSphere\" 1.5 Cryoablation Needle",
      "product_quantity": "39 units",
      "reason_for_recall": "Complaint trend regarding needle shaft gas leaks.",
      "recall_initiation_date": "20201118",
      "center_classification_date": "20201222",
      "report_date": "20201230",
      "code_info": "UPN: FPRPR3258     UDI: 07290104830211    Batch Number: A0125"
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