{
  "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": "Terminated",
      "city": "Aliso Viejo",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88024",
      "recalling_firm": "MICROVENTION INC.",
      "address_1": "35 Enterprise",
      "address_2": "N/A",
      "postal_code": "92656",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of FL, IA, MI, MN, TN and TX.",
      "recall_number": "Z-1829-2021",
      "product_description": "VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.",
      "product_quantity": "N/A",
      "reason_for_recall": "Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.",
      "recall_initiation_date": "20210421",
      "center_classification_date": "20210607",
      "termination_date": "20240216",
      "report_date": "20210616",
      "code_info": "Catalog Number: VIA-21-154-01  UDI: (01)00842429101650(11)191104(17)221031(10)19110403M  Lot Number: 19110403M"
    }
  ]
}