{
  "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": "2026-03-18",
    "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": "90528",
      "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": "Telephone",
      "distribution_pattern": "US distribution only - CA, CT, GA, IA, IL, IN, NY, OH, TX, WY",
      "recall_number": "Z-1491-2022",
      "product_description": "EkoSonic Kit 135cm, 12cm TZ    The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC components.  They are placed into the respective trays and sealed in a Tyvek pouch.  The sealed pouches are placed inside the kit carton (box) and the product labels.",
      "product_quantity": "10 units",
      "reason_for_recall": "Product may be mislabeled.",
      "recall_initiation_date": "20220525",
      "center_classification_date": "20220801",
      "report_date": "20220810",
      "code_info": "UPN: 500-56112    GTIN: 858593006264    Lot Numbers: 8035075263, 8035075264, 8035075265, 8035075266, 8035075267, 8035075268, 8035075269, 8035075270, 8035075271, 8035075272"
    }
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}