{
  "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": "90735",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "1 Scimed Pl",
      "address_2": "",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in the countries of Greece, France, Germany, Italy, Brazil and South Korea.  UPDATE:  The devices were also distributed to Russia.  There was no U.S. distribution.",
      "recall_number": "Z-1582-2022",
      "product_description": "Boston Scientific Guider Softip XF, 40 XF, 8F, Guide Catheter, REF H965100440",
      "product_quantity": "184 devices (UPDATED)",
      "reason_for_recall": "The impacted products were distributed with an MPXF tip curve shape instead of the 40XF tip curve shape for the Guider/40XF/8FR/90CM guide catheter.",
      "recall_initiation_date": "20220809",
      "center_classification_date": "20220825",
      "report_date": "20220831",
      "code_info": "UDI/DI 08714729202486, Lot/Batch 27339850, Use By 2021-05-18, and UPDATE:  Lot/Batch 29308869, Use By 4/27/2025.",
      "more_code_info": ""
    }
  ]
}