{
  "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": "2026-10-28",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cork",
      "state": "",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99906",
      "recalling_firm": "Boston Scientific Cork, Ltd.",
      "address_1": "Boston Scientific Limited, Business And Technology Park, Model Farm Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution   US Nationwide and territory of Puerto Rico. The countries of Albania, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Finland, France, Germany, Greece, Hungary, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Lithuania, Mexico, Moldova, Netherlands, New Zealand, Norway, Panama, PERU, Poland, Portugal, Qatar, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Tunisia, T¿rkiye, UAE, United Kingdom.",
      "recall_number": "Z-0223-2027",
      "product_description": "Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/1RO/105;  Material Number: M001195200",
      "product_quantity": "126",
      "reason_for_recall": "The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.",
      "recall_initiation_date": "20260916",
      "center_classification_date": "20261022",
      "report_date": "20261028",
      "code_info": "Material Number: M001195200; UDI-DI: 08714729839316; Batch Numbers: 37942457, 37999053, 38224527, 38304916, 38415911, 38687159, 38707977, 38916519, 39029416, 39029419, 39029640, 39092278, 40476286, 40479386, 40523958, 40525677;",
      "more_code_info": ""
    }
  ]
}